Ignite Creation Date:
2025-12-25 @ 3:27 AM
Ignite Modification Date:
2025-12-26 @ 2:08 AM
Study NCT ID:
NCT01895205
Status:
COMPLETED
Last Update Posted:
2015-08-19
First Post:
2013-06-26
Is NOT Gene Therapy:
False
Has Adverse Events:
False
Brief Title:
Treatment of Women After Severe Postpartum Haemorrhage
Sponsor:
Organization:
Raw JSON
{'hasResults': False, 'derivedSection': {'miscInfoModule': {'versionHolder': '2025-12-24'}, 'conditionBrowseModule': {'meshes': [{'id': 'D006473', 'term': 'Postpartum Hemorrhage'}], 'ancestors': [{'id': 'D007744', 'term': 'Obstetric Labor Complications'}, {'id': 'D011248', 'term': 'Pregnancy Complications'}, {'id': 'D005261', 'term': 'Female Urogenital Diseases and Pregnancy Complications'}, {'id': 'D000091642', 'term': 'Urogenital Diseases'}, {'id': 'D011644', 'term': 'Puerperal Disorders'}, {'id': 'D014592', 'term': 'Uterine Hemorrhage'}, {'id': 'D006470', 'term': 'Hemorrhage'}, {'id': 'D010335', 'term': 'Pathologic Processes'}, {'id': 'D013568', 'term': 'Pathological Conditions, Signs and Symptoms'}]}, 'interventionBrowseModule': {'meshes': [{'id': 'C557707', 'term': 'iron isomaltoside 1000'}, {'id': 'D017707', 'term': 'Erythrocyte Transfusion'}], 'ancestors': [{'id': 'D016913', 'term': 'Blood Component Transfusion'}, {'id': 'D001803', 'term': 'Blood Transfusion'}, {'id': 'D001691', 'term': 'Biological Therapy'}, {'id': 'D013812', 'term': 'Therapeutics'}]}}, 'protocolSection': {'designModule': {'phases': ['PHASE3'], 'studyType': 'INTERVENTIONAL', 'designInfo': {'allocation': 'RANDOMIZED', 'maskingInfo': {'masking': 'NONE'}, 'primaryPurpose': 'TREATMENT', 'interventionModel': 'PARALLEL'}, 'enrollmentInfo': {'type': 'ACTUAL', 'count': 13}}, 'statusModule': {'overallStatus': 'COMPLETED', 'startDateStruct': {'date': '2013-06'}, 'expandedAccessInfo': {'hasExpandedAccess': False}, 'statusVerifiedDate': '2015-08', 'completionDateStruct': {'date': '2015-08', 'type': 'ACTUAL'}, 'lastUpdateSubmitDate': '2015-08-18', 'studyFirstSubmitDate': '2013-06-26', 'studyFirstSubmitQcDate': '2013-07-04', 'lastUpdatePostDateStruct': {'date': '2015-08-19', 'type': 'ESTIMATED'}, 'studyFirstPostDateStruct': {'date': '2013-07-10', 'type': 'ESTIMATED'}, 'primaryCompletionDateStruct': {'date': '2015-08', 'type': 'ACTUAL'}}, 'outcomesModule': {'otherOutcomes': [{'measure': 'Change in anaemia symptoms', 'timeFrame': 'From Baseline to week 12'}, {'measure': 'Change in gastrointestinal symptoms', 'timeFrame': 'From Baseline to week 12'}], 'primaryOutcomes': [{'measure': 'Physical Fatigue', 'timeFrame': 'From exposure to 12 weeks post-exposure'}], 'secondaryOutcomes': [{'measure': 'Change in Hb concentration', 'timeFrame': 'From baseline to day 1, 2, 3, 4, 5, 6 and 7, week 3, 8 and 12'}, {'measure': 'Change in p-ferritin', 'timeFrame': 'From baseline to day 1, 2, 3, 4, 5, 6 and 7, week 3, 8 and 12'}, {'measure': 'Fatigue symptoms', 'timeFrame': 'from baseline to day 1, 2, 3, 4, 5, 6 and 7, week 3, 8 and 12'}, {'measure': 'Postpartum depression', 'timeFrame': 'From week 1 to 3, 8 and 12'}, {'measure': 'Breastfeeding', 'timeFrame': 'From exposure to 12 weeks post-exposure'}, {'measure': 'Number of adverse drug reactions (ADRs)', 'timeFrame': 'From baseline to day 1, 2, 3, 4, 5, 6 and 7, week 3, 8 and 12'}, {'measure': 'Change in p-iron', 'timeFrame': 'From baseline to day 1, 2, 3, 4, 5, 6 and 7, week 3, 8 and 12'}, {'measure': 'Change in p-transferrin', 'timeFrame': 'From baseline to day 1, 2, 3, 4, 5, 6 and 7, week 3, 8 and 12'}, {'measure': 'Change in transferrin saturation (TSAT)', 'timeFrame': 'From baseline to day 1, 2, 3, 4, 5, 6 and 7, week 3, 8 and 12'}, {'measure': 'Change in reticulocyte count', 'timeFrame': 'From baseline to day 1, 2, 3, 4, 5, 6 and 7, week 3, 8 and 12'}, {'measure': 'Change mean reticulocyte haemoglobin content (CHr)', 'timeFrame': 'From baseline to day 1, 2, 3, 4, 5, 6 and 7, week 3, 8 and 12'}]}, 'oversightModule': {'oversightHasDmc': False}, 'conditionsModule': {'conditions': ['Severe Postpartum Haemorrhage']}, 'descriptionModule': {'briefSummary': 'The primary purpose of this study is to get explorative information about IV high single dose infusion of iron isomaltoside 1000 compared to RBC transfusion in the treatment of severe PP-IDA evaluated as physical fatigue'}, 'eligibilityModule': {'sex': 'FEMALE', 'stdAges': ['ADULT', 'OLDER_ADULT'], 'minimumAge': '18 Years', 'healthyVolunteers': False, 'eligibilityCriteria': 'Inclusion Criteria:\n\n1. PPH \\> 1000 mL\n2. Hb ≥ 5.5 and ≤ 8.0 g/dL (≥ 3.5 and ≤ 5.0 mmol/L)\n3. Willingness to participate and signed the informed consent form\n\nExclusion Criteria:\n\n1. Women aged \\< 18 years\n2. Multiple births\n3. Peripartum RBC transfusion\n4. Known iron overload or disturbances in utilisation of iron (e.g. haemochromatosis and haemosiderosis)\n5. Known hypersensitivity to parenteral iron or any excipients in the investigational drug products\n6. Women with a history of active asthma within the last 5 years or a history of multiple allergies\n7. Known decompensated liver cirrhosis and active hepatitis\n8. Women with HELLP (Haemolysis Elevated Liver enzymes Low Platelet count) syndrome (defined according to "Dansk Selskab for Obstetrik og Gynækologi guidelines")\n9. Active acute infection assessed by clinical judgement\n10. Rheumatoid arthritis with symptoms or signs of active joint inflammation\n11. History of anaemia caused by e. g. thalassemia, hypersplenism or haemolytic anaemia (known haematologic disorder other than iron deficiency)\n12. Not able to read, speak and understand the Danish language\n13. Participation in any other clinical study where the study drug has not passed 5 half-lives prior to the baseline\n14. Any other medical condition that, in the opinion of Investigator, may cause the patient to be unsuitable for completion of the study or place the patient at potential risk from being in the study. For example, a malignancy, uncontrolled hypertension, unstable ischaemic heart disease or uncontrolled diabetes mellitus'}, 'identificationModule': {'nctId': 'NCT01895205', 'acronym': 'PP-02', 'briefTitle': 'Treatment of Women After Severe Postpartum Haemorrhage', 'organization': {'class': 'INDUSTRY', 'fullName': 'Pharmacosmos A/S'}, 'officialTitle': 'A Randomized Comparative, Open-Label Study of Intravenous Iron Isomaltoside 1000 (Monofer®) Administered by High Single Dose In-fusions or Red Blood Cell Transfusion in Women With Severe Postpartum Iron Deficiency Anaemia', 'orgStudyIdInfo': {'id': 'PP-02'}}, 'armsInterventionsModule': {'armGroups': [{'type': 'EXPERIMENTAL', 'label': 'Iron isomaltoside 1000', 'description': 'A single dose of 1500 mg iron isomaltoside 1000 is given. The dose is diluted in 100 ml 0.9% sodium chloride and given over approximately 15 min.', 'interventionNames': ['Drug: Iron isomaltoside 1000']}, {'type': 'ACTIVE_COMPARATOR', 'label': 'Red blood cell transfusion', 'description': 'Allogenic RBC transfusion is dosed to trigger Hb:\n\n* Women with Hb 5.5 - 6.4 g/dL (3.5-3.9 mmol/L) will receive 2 units of RBC\n* Women with Hb 6.5 - 8.0 g/dL (4.0-5.0 mmol/L) will receive 1 unit of RBC', 'interventionNames': ['Drug: Red blood cell transfusion']}], 'interventions': [{'name': 'Iron isomaltoside 1000', 'type': 'DRUG', 'otherNames': ['Monofer®'], 'armGroupLabels': ['Iron isomaltoside 1000']}, {'name': 'Red blood cell transfusion', 'type': 'DRUG', 'armGroupLabels': ['Red blood cell transfusion']}]}, 'contactsLocationsModule': {'locations': [{'city': 'Copenhagen', 'country': 'Denmark', 'geoPoint': {'lat': 55.67594, 'lon': 12.56553}}]}, 'sponsorCollaboratorsModule': {'leadSponsor': {'name': 'Pharmacosmos A/S', 'class': 'INDUSTRY'}, 'collaborators': [{'name': 'BioStata', 'class': 'INDUSTRY'}], 'responsibleParty': {'type': 'SPONSOR'}}}}