Coronary Heart Diseases Clinical Trial
— INDICOROfficial title:
The Paclitaxel-Eluting PTCA-Balloon Catheter in Combination With a Cobalt-Chromium Stent to Treat Coronary Artery Disease in a Real World Scenario
| Verified date | February 2016 |
| Source | Heart Centre Rotenburg |
| Contact | n/a |
| Is FDA regulated | No |
| Health authority | India: Institutional Review Board |
| Study type | Interventional |
The INDICOR study is a controlled, prospective, multicenter, randomized, two arm phase-II real world study assessing the acute, 6 months, and 12 months and 3 year outcome of cobalt-chromium stent (Coroflex Blue) deployment followed by Paclitaxel-eluting PTCA-balloon dilatation (SeQuent Please) and of Paclitaxel-eluting PTCA-balloon dilatation (SeQuent Please) followed by cobalt-chromium stent (Coroflex Blue) deployment for the treatment of de-novo and restenotic lesions in native coronary arteries. The study will be conducted in India.
| Status | Completed |
| Enrollment | 97 |
| Est. completion date | January 2016 |
| Est. primary completion date | September 2012 |
| Accepts healthy volunteers | No |
| Gender | Both |
| Age group | 18 Years and older |
| Eligibility |
Inclusion Criteria: - Patients with stable angina pectoris (CCS class 1-3) or with unstable angina pectoris (Braunwald class 1-2, A-C) or documented ischemia or with documented silent ischemia - Patients eligible for coronary revascularization by means of PCI - Patients suitable for coronary revascularization of any sort (balloon angioplasty, device-assisted balloon-angioplasty or coronary artery bypass grafting) - Patients must be older then 18 years of age - Women of childbearing potential may not be pregnant nor have the desire to becoming pregnant during the first year following the study procedure. Hence, patients will be advised to use an adequate birth control method up to and including 6 months follow-up. - Patients who are mentally and linguistically able to understand the aim of the study and to show sufficient compliance in following the study protocol - Patients must agree to undergo the 6 months angiographic follow-up - Patients must agree to undergo the 1 year and 3 year clinical follow-up Lesion Related (relates to up to 2 stenoses in two different coronary arteries to be treated per protocol) - Reference diameters ranging from 2.5 mm to 4.0 mm and length of stenosis from 10 mm to = 25 mm - Diameter stenosis pre procedure must be either more then 70 % or more then 50 % if ischemia corresponding to the target lesion is documented either by exercise stress ECG, stress echocardiography, or scintigraphy - Coverage of the target lesion must be intended and possible by a single Paclitaxel-eluting balloon Exclusion Criteria: Patient Related - Patients with acute (< 24 h) or recent (= 48 hours) myocardial infarction - Patients with unstable angina pectoris (Braunwald class 3) - Patients with severe congestive heart failure - Patients with severe heart failure NYHA IV - Patients demonstrating clinical signs of cardiogenic shock at the time of the procedure (systolic blood pressure of less than 80 mm Hg requiring inotropic support, IABP and/or fluid challenge). - Patients with severe valvular heart disease - Women who are pregnant or lactating - Patients with life expectancy of less than five years or factors making clinical follow-up difficult - Patients with bleeding diathesis in whom anticoagulation or anti-platelet medication is contraindicated - Patients who had a cerebral stroke < 6 months prior to the procedure - Patient participates in other clinical trials involving any investigational device or drug - Untreated hyperthyroidism - Patient has presence or history of severe renal failure (GFR<30ml/min) and is therefore not eligible for angiography. Patient's serum creatinine levels must be documented - Post transplantation of any organ or immune suppressive medication - Other disease to jeopardize follow-up (e.g., malignancy) - Addiction to any drug or to alcohol - Patients with any type of surgery during the week preceding the interventional procedure - Patients with percutaneous coronary intervention during the six months prior to enrollment into this study Lesion Related - Evidence of extensive thrombosis within target vessel before the intervention - Side branch > 2 mm in diameter originating from the lesion - Percutaneous coronary intervention of venous graft - Target segment is occluded of (i.e., acute or chronic) - In-stent restenosis (restenoses in non-stented segments are permitted) - Ostial lesion within 2 mm of vessel origin - Patients with another coronary stent implanted previously into the target vessel proximal to the target lesion |
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Subject), Primary Purpose: Treatment
| Country | Name | City | State |
|---|---|---|---|
| India | Upendra Kaul | New Delhi |
| Lead Sponsor | Collaborator |
|---|---|
| Ralf Degenhardt, PhD | B. Braun Melsungen AG |
India,
| Type | Measure | Description | Time frame | Safety issue |
|---|---|---|---|---|
| Primary | Late lumen loss at 6 months in-segment and in-stent for each treated coronary stenosis | 6 months | Yes |
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