Ignite Creation Date:
2025-12-24 @ 11:09 PM
Ignite Modification Date:
2026-01-02 @ 7:01 PM
Study NCT ID:
NCT04430569
Status:
RECRUITING
Last Update Posted:
2025-05-16
First Post:
2020-06-10
Is NOT Gene Therapy:
True
Has Adverse Events:
False
Brief Title:
Pulmonary Embolism International THrOmbolysis Study-3
Sponsor:
Organization:
Raw JSON
{'hasResults': False, 'derivedSection': {'miscInfoModule': {'versionHolder': '2025-12-24'}, 'conditionBrowseModule': {'meshes': [{'id': 'D011655', 'term': 'Pulmonary Embolism'}], 'ancestors': [{'id': 'D008171', 'term': 'Lung Diseases'}, {'id': 'D012140', 'term': 'Respiratory Tract Diseases'}, {'id': 'D004617', 'term': 'Embolism'}, {'id': 'D016769', 'term': 'Embolism and Thrombosis'}, {'id': 'D014652', 'term': 'Vascular Diseases'}, {'id': 'D002318', 'term': 'Cardiovascular Diseases'}]}, 'interventionBrowseModule': {'meshes': [{'id': 'D010959', 'term': 'Tissue Plasminogen Activator'}], 'ancestors': [{'id': 'D012697', 'term': 'Serine Endopeptidases'}, {'id': 'D010450', 'term': 'Endopeptidases'}, {'id': 'D010447', 'term': 'Peptide Hydrolases'}, {'id': 'D006867', 'term': 'Hydrolases'}, {'id': 'D004798', 'term': 'Enzymes'}, {'id': 'D045762', 'term': 'Enzymes and Coenzymes'}, {'id': 'D057057', 'term': 'Serine Proteases'}, {'id': 'D010960', 'term': 'Plasminogen Activators'}, {'id': 'D001779', 'term': 'Blood Coagulation Factors'}, {'id': 'D001798', 'term': 'Blood Proteins'}, {'id': 'D011506', 'term': 'Proteins'}, {'id': 'D000602', 'term': 'Amino Acids, Peptides, and Proteins'}, {'id': 'D001685', 'term': 'Biological Factors'}]}}, 'protocolSection': {'designModule': {'phases': ['PHASE3'], 'studyType': 'INTERVENTIONAL', 'designInfo': {'allocation': 'RANDOMIZED', 'maskingInfo': {'masking': 'TRIPLE', 'whoMasked': ['PARTICIPANT', 'CARE_PROVIDER', 'INVESTIGATOR']}, 'primaryPurpose': 'TREATMENT', 'interventionModel': 'PARALLEL'}, 'enrollmentInfo': {'type': 'ESTIMATED', 'count': 800}}, 'statusModule': {'overallStatus': 'RECRUITING', 'startDateStruct': {'date': '2021-08-04', 'type': 'ACTUAL'}, 'expandedAccessInfo': {'hasExpandedAccess': False}, 'statusVerifiedDate': '2025-05', 'completionDateStruct': {'date': '2028-08', 'type': 'ESTIMATED'}, 'lastUpdateSubmitDate': '2025-05-14', 'studyFirstSubmitDate': '2020-06-10', 'studyFirstSubmitQcDate': '2020-06-10', 'lastUpdatePostDateStruct': {'date': '2025-05-16', 'type': 'ACTUAL'}, 'studyFirstPostDateStruct': {'date': '2020-06-12', 'type': 'ACTUAL'}, 'primaryCompletionDateStruct': {'date': '2026-09', 'type': 'ESTIMATED'}}, 'outcomesModule': {'primaryOutcomes': [{'measure': 'Composite of (1) death from any cause or (2) hemodynamic decompensation or (3) objectively confirmed recurrent PE.', 'timeFrame': '30 days'}], 'secondaryOutcomes': [{'measure': 'Fatal or GUSTO severe or life threatening bleeding', 'timeFrame': '30 days'}, {'measure': 'Composite of the primary efficacy endpoint and GUSTO severe or life-threatening bleeding', 'timeFrame': '30 days', 'description': 'Assessment of net clinical benefit'}, {'measure': 'All-cause mortality', 'timeFrame': '30 days'}, {'measure': 'PE related death', 'timeFrame': '30 days'}, {'measure': 'Hemodynamic decompensation', 'timeFrame': '30 days'}, {'measure': 'Recurrent PE', 'timeFrame': '30 days'}, {'measure': 'Need for rescue thrombolysis, catheter-directed treatment or surgical embolectomy', 'timeFrame': '30 days'}, {'measure': 'Ischemic or hemorrhagic stroke', 'timeFrame': '30 days'}, {'measure': 'Serious adverse events', 'timeFrame': '30 days'}, {'measure': 'Persisting dyspnea', 'timeFrame': '180 days'}, {'measure': 'Persisting dyspnea', 'timeFrame': '2 years'}, {'measure': 'Persistent right ventricular dysfunction', 'timeFrame': '180 days'}, {'measure': 'Persistent right ventricular dysfunction', 'timeFrame': '2 years'}, {'measure': 'Functional outcome', 'timeFrame': '180 days'}, {'measure': 'Functional outcome', 'timeFrame': '2 years'}, {'measure': 'All-cause mortality', 'timeFrame': '2 years'}, {'measure': 'Confirmed chronic thromboembolic pulmonary hypertension', 'timeFrame': '2 years'}, {'measure': 'Utilization of health care ressources', 'timeFrame': '30 days', 'description': 'Questionnaire assessing the impact of the treatment on utilization of health care ressources'}, {'measure': 'Utilization of health care ressources', 'timeFrame': '180 days', 'description': 'Questionnaire assessing the impact of the treatment on utilization of health care ressources'}]}, 'oversightModule': {'oversightHasDmc': True, 'isFdaRegulatedDrug': False, 'isFdaRegulatedDevice': False}, 'conditionsModule': {'keywords': ['Intermediate-high-risk acute pulmonary embolism', 'Thrombolysis'], 'conditions': ['Pulmonary Embolism']}, 'referencesModule': {'references': [{'pmid': '24716681', 'type': 'BACKGROUND', 'citation': 'Meyer G, Vicaut E, Danays T, Agnelli G, Becattini C, Beyer-Westendorf J, Bluhmki E, Bouvaist H, Brenner B, Couturaud F, Dellas C, Empen K, Franca A, Galie N, Geibel A, Goldhaber SZ, Jimenez D, Kozak M, Kupatt C, Kucher N, Lang IM, Lankeit M, Meneveau N, Pacouret G, Palazzini M, Petris A, Pruszczyk P, Rugolotto M, Salvi A, Schellong S, Sebbane M, Sobkowicz B, Stefanovic BS, Thiele H, Torbicki A, Verschuren F, Konstantinides SV; PEITHO Investigators. Fibrinolysis for patients with intermediate-risk pulmonary embolism. N Engl J Med. 2014 Apr 10;370(15):1402-11. doi: 10.1056/NEJMoa1302097.'}, {'pmid': '29348184', 'type': 'BACKGROUND', 'citation': 'Barco S, Vicaut E, Klok FA, Lankeit M, Meyer G, Konstantinides SV; PEITHO Investigators. Improved identification of thrombolysis candidates amongst intermediate-risk pulmonary embolism patients: implications for future trials. Eur Respir J. 2018 Jan 18;51(1):1701775. doi: 10.1183/13993003.01775-2017. Print 2018 Jan. No abstract available.'}, {'pmid': '28335835', 'type': 'BACKGROUND', 'citation': 'Konstantinides SV, Vicaut E, Danays T, Becattini C, Bertoletti L, Beyer-Westendorf J, Bouvaist H, Couturaud F, Dellas C, Duerschmied D, Empen K, Ferrari E, Galie N, Jimenez D, Kostrubiec M, Kozak M, Kupatt C, Lang IM, Lankeit M, Meneveau N, Palazzini M, Pruszczyk P, Rugolotto M, Salvi A, Sanchez O, Schellong S, Sobkowicz B, Meyer G. Impact of Thrombolytic Therapy on the Long-Term Outcome of Intermediate-Risk Pulmonary Embolism. J Am Coll Cardiol. 2017 Mar 28;69(12):1536-1544. doi: 10.1016/j.jacc.2016.12.039.'}, {'pmid': '24917641', 'type': 'BACKGROUND', 'citation': 'Marti C, John G, Konstantinides S, Combescure C, Sanchez O, Lankeit M, Meyer G, Perrier A. Systemic thrombolytic therapy for acute pulmonary embolism: a systematic review and meta-analysis. Eur Heart J. 2015 Mar 7;36(10):605-14. doi: 10.1093/eurheartj/ehu218. Epub 2014 Jun 10.'}, {'pmid': '34560806', 'type': 'BACKGROUND', 'citation': 'Sanchez O, Charles-Nelson A, Ageno W, Barco S, Binder H, Chatellier G, Duerschmied D, Empen K, Ferreira M, Girard P, Huisman MV, Jimenez D, Katsahian S, Kozak M, Lankeit M, Meneveau N, Pruszczyk P, Petris A, Righini M, Rosenkranz S, Schellong S, Stefanovic B, Verhamme P, de Wit K, Vicaut E, Zirlik A, Konstantinides SV, Meyer G; PEITHO-3 Investigators. Reduced-Dose Intravenous Thrombolysis for Acute Intermediate-High-risk Pulmonary Embolism: Rationale and Design of the Pulmonary Embolism International THrOmbolysis (PEITHO)-3 trial. Thromb Haemost. 2022 May;122(5):857-866. doi: 10.1055/a-1653-4699. Epub 2021 Oct 31.'}]}, 'descriptionModule': {'briefSummary': 'In this study, we will assess the efficacy and safety of a reduced dose of thrombolytic therapy given in addition to low-molecular-weight heparin in patients with intermediate-high-risk acute pulmonary embolism. Half of participants will receive thrombolytic treatment, while the other half will receive a placebo.', 'detailedDescription': 'In patients with intermediate-risk pulmonary embolism, full-dose thrombolytic treatment was associated with a reduction in the combined risk of hemodynamic instability or death but was also associated with an increased risk of major and intracranial bleeding. Previous studies suggest that reduced dose of thrombolytic treatment may be as effective as the full dosage, but with a decreased risk of life-threatening bleeding. In this study, we will assess the efficacy and safety of a reduced dosage of thrombolytic therapy in patients with intermediate-high-risk acute pulmonary embolism.\n\nThe study is a randomized, placebo-controlled, double blind, multicenter, multinational trial with long-term follow-up.\n\nPatients fulfilling the inclusion criteria and without any of the exclusion criteria will be randomized within 6 hours after the investigator had confirmed the diagnosis.\n\nPatients will receive:\n\n* Alteplase (if randomized in the experimental group) or placebo (if randomized in the reference group) given within 30 minutes of randomization as a 15 min intravenous infusion at a dosage of 0.6 mg/kg with a total dose not exceeding 50 mg.\n* Parenteral anticoagulation with low molecular weight heparin, unfractionnated heparin or fondaparinux\n\nPrimary objective is to assess the efficacy of reduced dose thrombolytic therapy in patients with acute intermediate-high-risk pulmonary embolism at day 30.\n\nSecondary objectives are:\n\n1. To assess the safety of reduced dose thrombolytic therapy in patients with intermediate-high-risk acute pulmonary embolism at day 30\n2. To assess the net clinical benefit of reduced dose thrombolytic therapy in patients with intermediate-high-risk acute pulmonary embolism at day 30\n3. To assess the effect of reduced dose thrombolytic therapy on overall mortality of patients with intermediate-high-risk acute pulmonary embolism at day 30\n4. To assess the effect of reduced dose thrombolytic therapy on long-term mortality, functional impairment, residual right ventricular dysfunction and chronic thromboembolic pulmonary hypertension at 6 months and 2 years\n5. To assess the effect of reduced-dose thrombolytic therapy on utilization of health care resources at day 30 and day 180'}, 'eligibilityModule': {'sex': 'ALL', 'stdAges': ['ADULT', 'OLDER_ADULT'], 'minimumAge': '18 Years', 'healthyVolunteers': False, 'eligibilityCriteria': "Inclusion Criteria:\n\n* Age 18 years or older\n* Objectively confirmed acute PE with first symptoms occurring 2 weeks or less before randomization. Objective confirmation is based on at least one of the following criteria: (a) at least one segmental ventilation-perfusion mismatch on lung scanning; (b) a spiral computed tomography pulmonary angiography or pulmonary angiography showing a filling defect or an abrupt obstruction of a segmental or more proximal pulmonary artery\n* Acute PE confirmed within 24 hours prior to randomization\n* Elevated risk of early death, or of hemodynamic collapse, or PE recurrence, indicated by at least one of the following criteria: (a) systolic blood pressure ≤ 110 mm Hg over at least 15 minutes upon enrolment, (b) temporary need for fluid resuscitation and/or treatment with low-dose catecholamines, provided that the patient could be stabilized within 2 hours of admission and maintains SBP of ≥ 90 mmHg and adequate organ perfusion without catecholamine infusion; (c) respiratory rate \\> 20/min or oxygen saturation on pulse oximetry SpO2 \\<90% o(or partial arterial oxygen pressure \\< 60 mm Hg) at rest while breathing room air, (d) documented history of chronic symptomatic heart failure\n* Right ventricular dysfunction indicated by RV/LV diameter ratio \\>1.0 on echocardiography apical four-chamber or subcostal four-chamber view or on Computed Tomography Pulmonary Angiography (transverse plane)\n* Serum troponin I or T concentration above the upper limit of local normal using a high-sensitivity assay\n* Ability to randomize the patient within 6 hours after the investigator receives the results of the second of the two criteria for RV dysfunction (RV/LV diameter ratio \\>1.0) and myocardial injury (serum troponin I or T concentration above the upper limit of local normal), whichever comes latest.\n* Signed informed consent form\n\nExclusion Criteria:\n\n* Hemodynamic instability\n* Active bleeding\n* History of non-traumatic intracranial bleeding, any time\n* Acute ischemic stroke or transient ischemic attack (TIA) within the previous 6 months\n* Known central nervous system neoplasm/metastasis\n* Neurologic, ophthalmologic, abdominal, cardiac, thoracic, vascular or orthopedic surgery or trauma within 3 previous weeks\n* Platelet count \\< 100 G/L\n* INR \\> 1.4. If INR not available: prothrombin time ratio \\< 60%. If both INR and prothrombin time ratio are measured, INR is relevant for the assessment of this criterion.\n* Treatment with antiplatelet agents other than (a) acetylsalicylic acid (ASA) ≤ 100 mg once daily or (b) clopidogrel 75 mg once daily or (c) a single loading dose of ASA or clopidogrel. Dual antiplatelet therapy (ASA + clopidogrel) is not allowed.\n* Any direct oral anticoagulant within 12 hours of inclusion\n* Uncontrolled hypertension defined by SBP \\> 180 mm Hg at the time of inclusion\n* Known pericarditis or endocarditis\n* Known significant bleeding risk according to the investigator's judgement\n* Administration of thrombolytic agents within the previous 4 days\n* Vena cava filter insertion or pulmonary thrombectomy within the previous 4 days\n* Current participation in another interventional clinical study\n* Previous enrolment in this study\n* Known hypersensitivity to alteplase, gentamicin (a residue of the Actilyse® manufacturing process present in trace amounts), any of the excipients of Actilyse®, or low-molecular weight heparin (LMWH)\n* Known previous immune heparin-induced thrombocytopenia\n* Known severe liver disease (grade ≥ 3) including liver failure, cirrhosis, portal hypertension (esophageal varices) and active hepatitis\n* Acute symptomatic pancreatitis\n* Gastrointestinal ulcers or esophageal varices, documented within the past 3 months\n* Known arterial aneurysm, arterial or venous malformations\n* Pregnancy or parturition within the previous 30 days or current breastfeeding.\n* Women of childbearing potential who do not have a negative pregnancy test at the inclusion visit and do not use one of the following methods of birth control: hormonal contraception or intrauterine device or bilateral tubal occlusion\n* Any other condition that the investigator feels would place the patient at increased risk upon start of the investigational treatment\n* Life expectancy of less than 6 months or inability to complete 6-month follow-up.\n* Patient under legal protection"}, 'identificationModule': {'nctId': 'NCT04430569', 'acronym': 'PEITHO-3', 'briefTitle': 'Pulmonary Embolism International THrOmbolysis Study-3', 'organization': {'class': 'OTHER', 'fullName': 'Assistance Publique - Hôpitaux de Paris'}, 'officialTitle': 'A Reduced Dose of Thrombolytic Treatment for Patients With Intermediate High-risk Acute Pulmonary Embolism: a Randomized Controled Trial', 'orgStudyIdInfo': {'id': 'P160924'}, 'secondaryIdInfos': [{'id': 'P160924', 'type': 'OTHER', 'domain': 'Assistance Publique - Hôpitaux de Paris'}, {'id': 'PHRCN-16-0580', 'type': 'OTHER_GRANT', 'domain': 'French ministry of Health'}, {'id': '2018-000816-96', 'type': 'EUDRACT_NUMBER'}]}, 'armsInterventionsModule': {'armGroups': [{'type': 'EXPERIMENTAL', 'label': 'Alteplase', 'interventionNames': ['Drug: Alteplase']}, {'type': 'PLACEBO_COMPARATOR', 'label': 'Placebo', 'interventionNames': ['Drug: Placebo']}], 'interventions': [{'name': 'Alteplase', 'type': 'DRUG', 'description': 'Alteplase single intravenous infusion of 0.6 mg/kg of estimated bodyweight with a maximum of 50 mg given over 15 minutes.', 'armGroupLabels': ['Alteplase']}, {'name': 'Placebo', 'type': 'DRUG', 'description': 'Placebo single intravenous infusion of 0.6 mg/kg of estimated bodyweight with a maximum of 50 mg given over 15 minutes.', 'armGroupLabels': ['Placebo']}]}, 'contactsLocationsModule': {'locations': [{'zip': '8036', 'city': 'Graz', 'status': 'WITHDRAWN', 'country': 'Austria', 'facility': 'Graz, Mediz Universität', 'geoPoint': {'lat': 47.06733, 'lon': 15.44197}}, {'zip': '4020', 'city': 'Linz', 'status': 'RECRUITING', 'country': 'Austria', 'contacts': [{'name': 'Regina Steringer-Mascherbauer, MD', 'role': 'CONTACT', 'email': 'regina.steringer-mascherbauer@ordensklinikum.at'}], 'facility': 'Ordensklinikum Linz GmbH Elisabethinen', 'geoPoint': {'lat': 48.30639, 'lon': 14.28611}}, {'city': 'Brussels', 'status': 'NOT_YET_RECRUITING', 'country': 'Belgium', 'contacts': [{'name': 'Franck Verschuren, MD', 'role': 'CONTACT'}], 'facility': 'UCL Brussels', 'geoPoint': {'lat': 50.85045, 'lon': 4.34878}}, {'zip': '3000', 'city': 'Leuven', 'status': 'NOT_YET_RECRUITING', 'country': 'Belgium', 'contacts': [{'name': 'Thomas Vanassche, MD', 'role': 'CONTACT'}], 'facility': 'KU Leuven', 'geoPoint': {'lat': 50.87959, 'lon': 4.70093}}, {'zip': '4000', 'city': 'Liège', 'status': 'NOT_YET_RECRUITING', 'country': 'Belgium', 'contacts': [{'name': 'Alexandre Ghuysen, MD', 'role': 'CONTACT'}], 'facility': 'CHU Liège', 'geoPoint': {'lat': 50.63373, 'lon': 5.56749}}, {'city': 'Calgary', 'state': 'Alberta', 'status': 'NOT_YET_RECRUITING', 'country': 'Canada', 'contacts': [{'name': 'Kevin Solverson, MD', 'role': 'CONTACT'}], 'facility': 'Foothills Medical Centre', 'geoPoint': {'lat': 51.05011, 'lon': -114.08529}}, {'zip': 'ON L8V 1C3', 'city': 'Hamilton', 'state': 'Ontario', 'status': 'NOT_YET_RECRUITING', 'country': 'Canada', 'contacts': [{'name': 'Sam Schulman, MD', 'role': 'CONTACT', 'email': 'schulms@mcmaster.ca'}], 'facility': 'Juravinski Hospital - Hamilton Health Sciences Corporation', 'geoPoint': {'lat': 43.25011, 'lon': -79.84963}}, {'city': 'Hamilton', 'state': 'Ontario', 'status': 'NOT_YET_RECRUITING', 'country': 'Canada', 'contacts': [{'name': 'Sam Schulman, MD', 'role': 'CONTACT'}], 'facility': 'Hamilton General Hospital - Hamilton Health Sciences Corporation', 'geoPoint': {'lat': 43.25011, 'lon': -79.84963}}, {'city': 'Kingston', 'state': 'Ontario', 'status': 'NOT_YET_RECRUITING', 'country': 'Canada', 'contacts': [{'name': 'Kerstin de Wit, MD', 'role': 'CONTACT'}], 'facility': 'Kingston Health Sciences Centre', 'geoPoint': {'lat': 44.22976, 'lon': -76.48098}}, {'city': 'London', 'state': 'Ontario', 'status': 'NOT_YET_RECRUITING', 'country': 'Canada', 'contacts': [{'name': 'Justin Yan, MD', 'role': 'CONTACT'}], 'facility': 'London Health Sciences Centre', 'geoPoint': {'lat': 42.98339, 'lon': -81.23304}}, {'city': 'Ottawa', 'state': 'Ontario', 'status': 'NOT_YET_RECRUITING', 'country': 'Canada', 'contacts': [{'name': 'Lana Castellucci, MD', 'role': 'CONTACT'}], 'facility': 'The Ottawa Hopsital, General and Civic campuses', 'geoPoint': {'lat': 45.41117, 'lon': -75.69812}}, {'city': 'Montreal', 'state': 'Quebec', 'status': 'NOT_YET_RECRUITING', 'country': 'Canada', 'contacts': [{'name': 'Andrew Hirsch, MD', 'role': 'CONTACT'}], 'facility': 'Jewish General Hospital', 'geoPoint': {'lat': 45.50884, 'lon': -73.58781}}, {'zip': '49933', 'city': 'Angers', 'status': 'RECRUITING', 'country': 'France', 'contacts': [{'name': 'Pierre-Marie Roy, MD', 'role': 'CONTACT', 'email': 'pmroy@chu-angers.fr'}], 'facility': "CHU d'Angers", 'geoPoint': {'lat': 47.47156, 'lon': -0.55202}}, {'zip': '25030', 'city': 'Besançon', 'status': 'RECRUITING', 'country': 'France', 'contacts': [{'name': 'Nicolas Meneveau, MD', 'role': 'CONTACT', 'email': 'nicolas.meneveau@univ-fcomte.fr'}], 'facility': 'CHU de Besançon - Hôpital Jean-Minjoz', 'geoPoint': {'lat': 47.24878, 'lon': 6.01815}}, {'zip': '29000', 'city': 'Brest', 'status': 'RECRUITING', 'country': 'France', 'contacts': [{'name': 'Francis Couturaud, MD', 'role': 'CONTACT', 'email': 'francis.couturaud@chu-brest.fr'}], 'facility': 'CHU de Brest - Hôpital de la Cavale Blanche', 'geoPoint': {'lat': 48.39029, 'lon': -4.48628}}, {'zip': '37170', 'city': 'Chambray-lès-Tours', 'status': 'RECRUITING', 'country': 'France', 'contacts': [{'name': 'Denis Angoulvant, MD', 'role': 'CONTACT', 'email': 'd.angoulvant@chu-tours.fr'}], 'facility': 'CHU de Tours - Hôpital Trousseau', 'geoPoint': {'lat': 47.33537, 'lon': 0.70286}}, {'zip': '63000', 'city': 'Clermont-Ferrand', 'status': 'RECRUITING', 'country': 'France', 'contacts': [{'name': 'Jeannot Schmidt, MD', 'role': 'CONTACT', 'email': 'jschmidt@chu-clermontferrand.fr'}], 'facility': 'CHU de Clermont-Ferrand - Hôpital Gabriel Montpied', 'geoPoint': {'lat': 45.77969, 'lon': 3.08682}}, {'zip': '94010', 'city': 'Créteil', 'status': 'RECRUITING', 'country': 'France', 'contacts': [{'name': 'Pascal Lim, MD', 'role': 'CONTACT', 'email': 'pascal.lim@aphp.fr'}], 'facility': 'AP-HP - hôpital Henri-Mondor', 'geoPoint': {'lat': 48.79266, 'lon': 2.46569}}, {'zip': '38700', 'city': 'La Tronche', 'status': 'RECRUITING', 'country': 'France', 'contacts': [{'name': 'Hélène Bouvaist, MD', 'role': 'CONTACT', 'email': 'hbouvaist@chu-grenoble.fr'}], 'facility': 'CHU de Grenoble - Hôpital Michallon', 'geoPoint': {'lat': 45.20507, 'lon': 5.74629}}, {'zip': '94270', 'city': 'Le Kremlin-Bicêtre', 'status': 'RECRUITING', 'country': 'France', 'contacts': [{'name': 'Laurent Savale, MD', 'role': 'CONTACT'}], 'facility': 'AP-HP - hôpital Bicêtre', 'geoPoint': {'lat': 48.81471, 'lon': 2.36073}}, {'zip': '59000', 'city': 'Lille', 'status': 'WITHDRAWN', 'country': 'France', 'facility': 'CHU de Lille - Institut Cœur Poumon', 'geoPoint': {'lat': 50.63391, 'lon': 3.05512}}, {'zip': '69000', 'city': 'Lyon', 'status': 'WITHDRAWN', 'country': 'France', 'facility': 'HCL - Hôpital Edouard Herriot', 'geoPoint': {'lat': 45.74906, 'lon': 4.84789}}, {'zip': '69000', 'city': 'Lyon', 'status': 'RECRUITING', 'country': 'France', 'contacts': [{'name': 'Laurent Argaud, MD', 'role': 'CONTACT', 'email': 'laurent.argaud@chu-lyon.fr'}], 'facility': 'HCL - Hôpital Edouard Herriot', 'geoPoint': {'lat': 45.74906, 'lon': 4.84789}}, {'zip': '69495', 'city': 'Lyon', 'status': 'RECRUITING', 'country': 'France', 'contacts': [{'name': 'Donatien De Marignan', 'role': 'CONTACT', 'email': 'donatien.de-marignan@chu-lyon.fr', 'phone': '04 78 86 21 18'}], 'facility': 'HCL - Centre Hospitalier Lyon-Sud, Pierre-Bénite', 'geoPoint': {'lat': 45.74906, 'lon': 4.84789}}, {'zip': '13000', 'city': 'Marseille', 'status': 'RECRUITING', 'country': 'France', 'contacts': [{'name': 'Gabrielle Sarlon-Bartoli, MD', 'role': 'CONTACT', 'email': 'gabrielle.sarlon@ap-hm.fr'}], 'facility': 'AP-HM - Hôpital de la Timone', 'geoPoint': {'lat': 43.29695, 'lon': 5.38107}}, {'zip': '34000', 'city': 'Montpellier', 'status': 'WITHDRAWN', 'country': 'France', 'facility': 'CHU de Montpellier - Hôpital Lapeyronie', 'geoPoint': {'lat': 43.61093, 'lon': 3.87635}}, {'zip': '06000', 'city': 'Nice', 'status': 'TERMINATED', 'country': 'France', 'facility': 'CHU de Nice - Hôpital Pasteur', 'geoPoint': {'lat': 43.70313, 'lon': 7.26608}}, {'zip': '75010', 'city': 'Paris', 'status': 'WITHDRAWN', 'country': 'France', 'facility': 'AP-HP - Hôpital Lariboisière', 'geoPoint': {'lat': 48.85341, 'lon': 2.3488}}, {'zip': '75015', 'city': 'Paris', 'status': 'RECRUITING', 'country': 'France', 'contacts': [{'name': 'Benjamin Planquette, MD', 'role': 'CONTACT', 'email': 'benjamin.planquette@aphp.fr'}], 'facility': 'AP-HP - hôpital européen Georges-Pompidou', 'geoPoint': {'lat': 48.85341, 'lon': 2.3488}}, {'zip': '75018', 'city': 'Paris', 'status': 'RECRUITING', 'country': 'France', 'contacts': [{'name': 'Grégory Ducrocq, MD', 'role': 'CONTACT', 'email': 'gregory.ducrocq@aphp.fr'}], 'facility': 'AP-HP - Hôpital Bichat-Claude-Bernard', 'geoPoint': {'lat': 48.85341, 'lon': 2.3488}}, {'zip': '75020', 'city': 'Paris', 'status': 'RECRUITING', 'country': 'France', 'contacts': [{'name': 'Aude Gibelin, MD', 'role': 'CONTACT', 'email': 'aude.gibelin@aphp.fr'}], 'facility': 'AP-HP - Hôpital Tenon', 'geoPoint': {'lat': 48.85341, 'lon': 2.3488}}, {'zip': '69495', 'city': 'Pierre-Bénite', 'status': 'WITHDRAWN', 'country': 'France', 'facility': 'HCL - Centre Hospitalier Lyon-Sud', 'geoPoint': {'lat': 45.70359, 'lon': 4.82424}}, {'zip': '42055', 'city': 'Saint-Etienne', 'status': 'RECRUITING', 'country': 'France', 'contacts': [{'name': 'Laurent Bertoletti, MD', 'role': 'CONTACT', 'email': 'laurent.bertoletti@chu-st-etienne.fr'}], 'facility': 'CHU de Saint-Étienne - Hôpital Nord', 'geoPoint': {'lat': 45.43389, 'lon': 4.39}}, {'zip': '67000', 'city': 'Strasbourg', 'status': 'RECRUITING', 'country': 'France', 'contacts': [{'name': 'Patrick Ohlmann, MD', 'role': 'CONTACT', 'email': 'patrick.ohlmann@chu-strasbourg.fr'}], 'facility': 'CHU de Strasbourg - Hôpital Civil', 'geoPoint': {'lat': 48.58392, 'lon': 7.74553}}, {'zip': '31000', 'city': 'Toulouse', 'status': 'RECRUITING', 'country': 'France', 'contacts': [{'name': 'Caroline Biendel-Piquet, MD', 'role': 'CONTACT', 'email': 'biendel.c@chu-toulouse.fr'}], 'facility': 'CHU de Toulouse - Hôpital Rangueil', 'geoPoint': {'lat': 43.60426, 'lon': 1.44367}}, {'zip': '79189', 'city': 'Bad Krozingen', 'status': 'RECRUITING', 'country': 'Germany', 'contacts': [{'name': 'Philipp Breitbart, MD', 'role': 'CONTACT', 'email': 'philipp.breitbart@uniklinik-freiburg.de'}], 'facility': 'Universitäts-Herzzentrum Freiburg - 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