Ignite Creation Date:
2025-12-24 @ 6:43 PM
Ignite Modification Date:
2025-12-30 @ 9:47 PM
Study NCT ID:
NCT00235157
Status:
COMPLETED
Last Update Posted:
2008-08-06
First Post:
2005-10-06
Is NOT Gene Therapy:
True
Has Adverse Events:
False
Brief Title:
A Comparison of Coated and Uncoated Stents in Renal Artery Treatment.
Sponsor:
Organization:
Raw JSON
{'hasResults': False, 'derivedSection': {'miscInfoModule': {'versionHolder': '2025-12-24'}, 'conditionBrowseModule': {'meshes': [{'id': 'D012078', 'term': 'Renal Artery Obstruction'}], 'ancestors': [{'id': 'D007674', 'term': 'Kidney Diseases'}, {'id': 'D014570', 'term': 'Urologic Diseases'}, {'id': 'D052776', 'term': 'Female Urogenital Diseases'}, {'id': 'D005261', 'term': 'Female Urogenital Diseases and Pregnancy Complications'}, {'id': 'D000091642', 'term': 'Urogenital Diseases'}, {'id': 'D052801', 'term': 'Male Urogenital Diseases'}, {'id': 'D001157', 'term': 'Arterial Occlusive Diseases'}, {'id': 'D014652', 'term': 'Vascular Diseases'}, {'id': 'D002318', 'term': 'Cardiovascular Diseases'}]}}, 'protocolSection': {'designModule': {'phases': ['PHASE2'], 'studyType': 'INTERVENTIONAL', 'designInfo': {'allocation': 'NON_RANDOMIZED', 'maskingInfo': {'masking': 'NONE'}, 'primaryPurpose': 'TREATMENT', 'interventionModel': 'SINGLE_GROUP'}, 'enrollmentInfo': {'type': 'ACTUAL', 'count': 105}}, 'statusModule': {'overallStatus': 'COMPLETED', 'startDateStruct': {'date': '2001-11'}, 'expandedAccessInfo': {'hasExpandedAccess': False}, 'statusVerifiedDate': '2008-08', 'completionDateStruct': {'date': '2005-07', 'type': 'ACTUAL'}, 'lastUpdateSubmitDate': '2008-08-05', 'studyFirstSubmitDate': '2005-10-06', 'studyFirstSubmitQcDate': '2005-10-07', 'lastUpdatePostDateStruct': {'date': '2008-08-06', 'type': 'ESTIMATED'}, 'studyFirstPostDateStruct': {'date': '2005-10-10', 'type': 'ESTIMATED'}, 'primaryCompletionDateStruct': {'date': '2002-11', 'type': 'ACTUAL'}}, 'outcomesModule': {'primaryOutcomes': [{'measure': 'assessment of the angiographical in-stent minimal lumen diameter', 'timeFrame': '6-months follow up'}], 'secondaryOutcomes': [{'measure': 'clinical primary patency', 'timeFrame': 'discharge, 1, 6 and 12 months post-procedure'}, {'measure': 'procedural success', 'timeFrame': 'post-procedure'}, {'measure': 'worsening renal function', 'timeFrame': '30 days, 6 months, 12 months'}, {'measure': 'change in blood pressure measurement', 'timeFrame': '30 days, 6 months, 12 months'}, {'measure': 'significant embolic events causing end-organ damage', 'timeFrame': '30 days, 6 months, and 12 months'}]}, 'oversightModule': {'oversightHasDmc': True}, 'conditionsModule': {'conditions': ['Renal Artery Stenosis']}, 'referencesModule': {'references': [{'pmid': '17696619', 'type': 'RESULT', 'citation': 'Zahringer M, Sapoval M, Pattynama PM, Rabbia C, Vignali C, Maleux G, Boyer L, Szczerbo-Trojanowska M, Jaschke W, Hafsahl G, Downes M, Beregi JP, Veeger NJ, Stoll HP, Talen A. Sirolimus-eluting versus bare-metal low-profile stent for renal artery treatment (GREAT Trial): angiographic follow-up after 6 months and clinical outcome up to 2 years. J Endovasc Ther. 2007 Aug;14(4):460-8. doi: 10.1177/152660280701400405.'}]}, 'descriptionModule': {'briefSummary': 'The primary objective of this study is to compare the safety and performance of the Palmaz Genesis™ balloon expandable stent, with or without sirolimus coating in the treatment of renal artery stenosis, measured at 6 months follow up via angiography.', 'detailedDescription': 'Multi-center, prospective, controlled, non-randomized investigational feasibility study. One hundred (100) patients with de novo or restenotic renal artery lesions consisting of \\>= 50% stenosis and reference vessel of \\>= 4.0 to \\<= 8.0 mm in diameter will be sequentially included, 50 without sirolimus coating, followed by 50 with sirolimus coating Palmaz GenesisTM. Patients will be followed for 24 months post-procedure, with all patients having clinical assessments at discharge, 1,6, 12 and 24 months. This study will be conducted at twelve investigational sites.\n\nIt is anticipated that the total length of time required to complete the study will be 46 months.'}, 'eligibilityModule': {'sex': 'ALL', 'stdAges': ['ADULT', 'OLDER_ADULT'], 'minimumAge': '30 Years', 'healthyVolunteers': False, 'eligibilityCriteria': 'Inclusion Criteria:\n\n1. Clinical indication for renal artery revascularization of atherosclerotic renal artery stenosis \\>=50% as measured by operator or estimated original vessel diameter, based on healthy vessel segment and contralateral side.\n2. The reference vessel renal artery must be \\>= 4mm and \\<= 8 mm by visual estimate.\n3. The patient must have a baseline serum creatinine of \\<= 5.0 mg/dl.\n\nExclusion Criteria:\n\n1. Total occlusion of the renal artery.\n2. Lesions which would require more than 2 stents.\n3. Lesions which are in arteries to transplanted or bypassed kidneys.\n4. Abdominal aortic aneurysm \\> 4.0 cm in diameter.\n5. Patients with ASA classification \\>=4.'}, 'identificationModule': {'nctId': 'NCT00235157', 'acronym': 'GREAT', 'briefTitle': 'A Comparison of Coated and Uncoated Stents in Renal Artery Treatment.', 'organization': {'class': 'INDUSTRY', 'fullName': 'Cordis US Corp.'}, 'officialTitle': 'Palmaz Genesis Peripheral Stainless Steel Balloon Expandable Stent, Comparing a Sirolimus Coated Versus an Uncoated Stent in REnal Artery Treatment.', 'orgStudyIdInfo': {'id': 'EE01-01'}}, 'armsInterventionsModule': {'armGroups': [{'type': 'EXPERIMENTAL', 'label': '1', 'description': 'Sirolimus-eluting Palmaz Genesis peripheral stent', 'interventionNames': ['Device: Sirolimus-eluting Palmaz Genesis peripheral stent']}], 'interventions': [{'name': 'Sirolimus-eluting Palmaz Genesis peripheral stent', 'type': 'DEVICE', 'otherNames': ['Palmaz Genesis Stent'], 'description': 'treatment of renal artery stenosis with a renal stent', 'armGroupLabels': ['1']}]}, 'contactsLocationsModule': {'locations': [{'zip': '75 015', 'city': 'Paris', 'country': 'France', 'facility': 'Hopital Européen Georges Pompidou', 'geoPoint': {'lat': 48.85341, 'lon': 2.3488}}, {'zip': '50931', 'city': 'Cologne', 'country': 'Germany', 'facility': 'Universitätskliniken Köln', 'geoPoint': {'lat': 50.93333, 'lon': 6.95}}, {'zip': '3000 CA', 'city': 'Rotterdam', 'country': 'Netherlands', 'facility': 'Erasmus MC Rotterdam', 'geoPoint': {'lat': 51.9225, 'lon': 4.47917}}], 'overallOfficials': [{'name': 'Markus Zähringer, MD', 'role': 'PRINCIPAL_INVESTIGATOR', 'affiliation': 'Universitätskliniken Köln'}, {'name': 'Marc Sapoval, MD', 'role': 'PRINCIPAL_INVESTIGATOR', 'affiliation': 'Hopital Européen Georges Pompidou'}, {'name': 'Peter M Pattynama, MD', 'role': 'PRINCIPAL_INVESTIGATOR', 'affiliation': 'Erasmus MC Rotterdam'}]}, 'sponsorCollaboratorsModule': {'leadSponsor': {'name': 'Cordis US Corp.', 'class': 'INDUSTRY'}, 'responsibleParty': {'oldNameTitle': 'Dr. Hans-Peter Stoll, Director Clinical Affairs', 'oldOrganization': 'Cordis'}}}}