Ignite Creation Date:
2025-12-24 @ 9:57 PM
Ignite Modification Date:
2025-12-25 @ 7:35 PM
Study NCT ID:
NCT03423732
Status:
UNKNOWN
Last Update Posted:
2021-04-09
First Post:
2018-01-25
Is NOT Gene Therapy:
False
Has Adverse Events:
False
Brief Title:
Cardiovascular Clinical Project to Evaluate the Regenerative Capacity of CardioCell in Patients With No-option Critical Limb Ischemia (N-O CLI)
Sponsor:
Organization:
Raw JSON
{'hasResults': False, 'derivedSection': {'miscInfoModule': {'versionHolder': '2025-12-24'}, 'conditionBrowseModule': {'meshes': [{'id': 'D000089802', 'term': 'Chronic Limb-Threatening Ischemia'}], 'ancestors': [{'id': 'D058729', 'term': 'Peripheral Arterial Disease'}, {'id': 'D050197', 'term': 'Atherosclerosis'}, {'id': 'D001161', 'term': 'Arteriosclerosis'}, {'id': 'D001157', 'term': 'Arterial Occlusive Diseases'}, {'id': 'D014652', 'term': 'Vascular Diseases'}, {'id': 'D002318', 'term': 'Cardiovascular Diseases'}, {'id': 'D016491', 'term': 'Peripheral Vascular Diseases'}, {'id': 'D002908', 'term': 'Chronic Disease'}, {'id': 'D020969', 'term': 'Disease Attributes'}, {'id': 'D010335', 'term': 'Pathologic Processes'}, {'id': 'D013568', 'term': 'Pathological Conditions, Signs and Symptoms'}, {'id': 'D007511', 'term': 'Ischemia'}]}}, 'protocolSection': {'designModule': {'phases': ['PHASE2', 'PHASE3'], 'studyType': 'INTERVENTIONAL', 'designInfo': {'allocation': 'RANDOMIZED', 'maskingInfo': {'masking': 'QUADRUPLE', 'whoMasked': ['PARTICIPANT', 'CARE_PROVIDER', 'INVESTIGATOR', 'OUTCOMES_ASSESSOR'], 'maskingDescription': 'The Data and Safety Monitoring Board (DSMB) will be blinded at project start, but may request unblinding if necessary to accommodate effective review of data.\n\nOther than the DSMB (if necessary), the only other "un-blinded parties", meaning that they will have knowledge as to the patient\'s treatment assignment, will be the PBTiK UJ CM employee who participates in randomization utilizing randomization lists and investigational medication preparation.'}, 'primaryPurpose': 'TREATMENT', 'interventionModel': 'PARALLEL', 'interventionModelDescription': 'The N-O CLI trial will enroll 105 patients with randomization into active and sham therapy with 2:1 ratio.\n\nAdditional 5-10 subjects meeting inclusion/exclusion criteria will receive, in a non-blinded fashion, labelled CardioCell to determine the early uptake and retention of IMP in the target ischemic tissues.'}, 'enrollmentInfo': {'type': 'ACTUAL', 'count': 50}}, 'statusModule': {'overallStatus': 'UNKNOWN', 'lastKnownStatus': 'ACTIVE_NOT_RECRUITING', 'startDateStruct': {'date': '2018-04-19', 'type': 'ACTUAL'}, 'expandedAccessInfo': {'hasExpandedAccess': False}, 'statusVerifiedDate': '2021-04', 'completionDateStruct': {'date': '2021-09-30', 'type': 'ESTIMATED'}, 'lastUpdateSubmitDate': '2021-04-08', 'studyFirstSubmitDate': '2018-01-25', 'studyFirstSubmitQcDate': '2018-02-05', 'lastUpdatePostDateStruct': {'date': '2021-04-09', 'type': 'ACTUAL'}, 'studyFirstPostDateStruct': {'date': '2018-02-06', 'type': 'ACTUAL'}, 'primaryCompletionDateStruct': {'date': '2021-05-31', 'type': 'ESTIMATED'}}, 'outcomesModule': {'primaryOutcomes': [{'measure': 'Change in pain-free walking distance', 'timeFrame': '6 month FU', 'description': 'Change in pain-free walking distance (6M FU vs index evaluation) between two groups (active vs placebo therapy).'}], 'secondaryOutcomes': [{'measure': 'Amputation-free survival period', 'timeFrame': '6 month and 1 year FU.', 'description': 'Amputation-free survival period evaluation of treated leg at 6 month and 1 year FU.'}, {'measure': 'Ulcer-free survival', 'timeFrame': '6 month and 1 year FU', 'description': 'Ulcer-free survival (in patients without ulceration at baseline evaluation) of treated leg in period evaluation at 6 month and 1 year FU.'}, {'measure': 'Ulcer-extension free survival', 'timeFrame': '6 month and 1 year FU', 'description': 'Ulcer-extension free survival (in patients with ulceration in the beginning of the trial) of treated leg in period evaluation at 6 month and 1 year FU.'}, {'measure': 'Change in tissue oxygen/CO2 tension', 'timeFrame': '45 days, 3 month, 6 month and 1 year FU', 'description': 'Change in tissue oxygen/CO2 tension, assessed by NIRS method at each trial evaluation point.'}, {'measure': 'An improvement of tissue perfusion', 'timeFrame': '45 days, 3 month, 6 month and 1 year FU', 'description': 'An improvement of tissue perfusion assessed in MRI at each trial evaluation point.'}, {'measure': 'Change in transcutaneous pressure of O2', 'timeFrame': '45 days, 3 month, 6 month and 1 year FU', 'description': 'Change in transcutaneous pressure of O2 (tcpO2) between two groups (active vs placebo therapy) at each trial evaluation point.'}, {'measure': 'Change in ABI score', 'timeFrame': '45 days, 3 month, 6 month and 1 year FU', 'description': 'Change in ABI score at each trial evaluation point.\n\nThe ankle-brachial index (ABI) is the ratio of the blood pressure at the ankle to the blood pressure in the upper arm and is calculated by dividing the systolic blood pressure at the ankle by the systolic blood pressure in the arm.\n\nAn ABI between and including 0.9 and 1.2 is considered normal, while a lesser than 0.9 indicates peripheral arterial disease. An ABI value of 1.3 or greater is also considered abnormal, and suggests calcification of the walls of the arteries and incompressible vessels. ABI score progression towards the normal range is considered as a better outcome.'}, {'measure': 'Quality of life improvement, assessed by SF-36 questionnaire', 'timeFrame': '45 days, 3 month, 6 month and 1 year FU', 'description': 'Quality of life improvement, assessed by SF-36 questionnaire or other dedicated for investigated population at each trial evaluation point.'}]}, 'oversightModule': {'oversightHasDmc': True, 'isFdaRegulatedDrug': False, 'isFdaRegulatedDevice': False}, 'conditionsModule': {'conditions': ['Critical Limb Ischemia']}, 'descriptionModule': {'briefSummary': 'The main objective of the CIRCULATE project is to compare the clinical outcomes of CardioCell administration in treatment of ischemic damages of cardiovascular system with control group, who will be treated by the administration of placebo during the sham procedure.', 'detailedDescription': 'It is planned to enroll 105 patients into N-O CLI trial with randomization into active (CardioCell) therapy and sham procedure/placebo administration with 2:1 ratio.\n\nThe primary research question of this project is to check if the administration of CardioCell could improve the clinical outcomes in patients with N-O CLI.\n\nThere are several secondary questions, defined by secondary endpoints, e.g.: if the investigated treatment is possible to administered, if the investigated treatment is safe in each studied indication and way of CardioCell administration, if it is possible to define any selected subgroup in which the treatment results are significantly different than in whole group.'}, 'eligibilityModule': {'sex': 'ALL', 'stdAges': ['ADULT', 'OLDER_ADULT'], 'maximumAge': '80 Years', 'minimumAge': '18 Years', 'healthyVolunteers': False, 'eligibilityCriteria': "Inclusion Criteria:\n\n* Patients able to walk\n* Male and female patients, aged 18-80 years\n* No-option CLI (definition: exhausted revascularization options including surgery or endovascular treatment) in Rutherford stage 4-5\n* In case of bilateral N-O CLI, the limb with shorter claudication distance will be treated\n* Presence of adequate inflow (patent iliac and common femoral arteries)\n* Run-off through at least one (even partially seen) below-the-knee (BTK) artery\n* Signed informed consent\n\nExclusion Criteria:\n\n* Malignancy\n* Moderate or severe immunodeficiency\n* Acute or chronic bacterial or viral infectious disease\n* Soft tissue disease or local infection in a place of required artery puncture\n* Pregnancy or breastfeeding\n* Any objective or subjective reason for inability to attend follow-up visits\n* Females of childbearing potential, who does not want to use a highly effective method of contraception\n* Females of childbearing potential who does not have a menstrual period confirmed and a negative highly sensitive urine or serum pregnancy test\n* Participation in any other clinical research study that has not reached the primary efficacy endpoint or otherwise would interfere with the patient's participation in this project\n* Life expectancy \\< 1 year\n* Any concurrent disease or condition that, in the opinion of the investigator, would make the patient unsuitable for participation in the project"}, 'identificationModule': {'nctId': 'NCT03423732', 'briefTitle': 'Cardiovascular Clinical Project to Evaluate the Regenerative Capacity of CardioCell in Patients With No-option Critical Limb Ischemia (N-O CLI)', 'organization': {'class': 'OTHER', 'fullName': 'John Paul II Hospital, Krakow'}, 'officialTitle': "Regeneration of Ischemic Damages in Cardiovascular System Using Wharton's Jelly as an Unlimited Source of Mesenchymal Stem Cells for Regenerative Medicine. Project of the National Centre for Research and Development (Poland) 'STRATEGMED II'. Cardiovascular Clinical Project to Evaluate the Regenerative Capacity of CardioCell in Patients With No-option Critical Limb Ischemia (N-O CLI)", 'orgStudyIdInfo': {'id': 'CardioCell in N-O CLI'}}, 'armsInterventionsModule': {'armGroups': [{'type': 'ACTIVE_COMPARATOR', 'label': 'Active Group', 'description': 'Patients randomized to the active treatment group will receive CardioCell consist 30 000 000 cells (suspended in 20 ml of 0.9% NaCl and 5% albumin); 15 000 000 via common femoral artery injection and 15 000 000 via intramuscular injections above the knee (ATK, 6 injection sites) and below the knee (BTK, 6 injection sites).', 'interventionNames': ['Drug: CardioCell']}, {'type': 'PLACEBO_COMPARATOR', 'label': 'Control Group', 'description': 'Patients randomized to the placebo group will receive Placebos consist 0.9% NaCl and 5% albumin injections (in the same volumes as CardioCell) injections in the same manner.', 'interventionNames': ['Drug: Placebos']}], 'interventions': [{'name': 'CardioCell', 'type': 'DRUG', 'otherNames': ['CardioCell administration'], 'description': 'Patients in the N-O CLI trial will receive a full dose of IMP three times during the trial: at baseline, after 45 days post index administration and after 3 months post index administration.\n\nIMP will be administered into femoral artery and intramuscularly with 50:50 proportion. The intramuscularly dose will be administered into muscles above and below the knee in 50:50 proportion.', 'armGroupLabels': ['Active Group']}, {'name': 'Placebos', 'type': 'DRUG', 'otherNames': ['Placebo administration'], 'description': 'Patients randomized to the control group will receive 0.9% NaCl and 5% albumin injections (in the same volume as CardioCell) in the same manner.\n\nControl group will receive the same amount of fluid used for WJMSCs preparation, without cells.', 'armGroupLabels': ['Control Group']}]}, 'contactsLocationsModule': {'locations': [{'zip': '40-635', 'city': 'Katowice', 'country': 'Poland', 'facility': 'Leszek Giec Upper-Silesian Medical Centre of the Silesian Medical University in Katowice', 'geoPoint': {'lat': 50.2597, 'lon': 19.02173}}, {'zip': '31-202', 'city': 'Krakow', 'country': 'Poland', 'facility': 'The John Paul II Hospital', 'geoPoint': {'lat': 50.06143, 'lon': 19.93658}}], 'overallOfficials': [{'name': 'Mariusz Trystuła, MD', 'role': 'PRINCIPAL_INVESTIGATOR', 'affiliation': 'John Paul II Hospital'}]}, 'sponsorCollaboratorsModule': {'leadSponsor': {'name': 'John Paul II Hospital, Krakow', 'class': 'OTHER'}, 'collaborators': [{'name': 'KCRI', 'class': 'OTHER'}, {'name': 'National Center for Research and Development, Poland', 'class': 'OTHER'}], 'responsibleParty': {'type': 'SPONSOR'}}}}