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NCT00180271 · ClinicalTrials.gov registry record · NA
MADIT-CRT: Multicenter Automatic Defibrillator Implantation With Cardiac Resynchronization Therapy
A NA study of Congestive Heart Failure and Tachycardia, sponsored by Boston Scientific Corporation.
- Completed
- Registry status
- NA
- Development phase
- 1,820
- Enrollment target
- 1
- Study location
NCT00180271: Completed NA study of Congestive Heart Failure and Tachycardia, sponsored by Boston Scientific Corporation.
NCT00180271 is a NA study of Congestive Heart Failure and Tachycardia that has completed, run by Boston Scientific Corporation. The registered enrollment target is 1,820 participants, above the 294-participant average among 51 other Congestive Heart Failure trials with a reported enrollment target (519% higher). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT00180271, a NA study of Congestive Heart Failure and Tachycardia, has completed, sponsored by Boston Scientific Corporation.
- COMPLETED
- Registry status
- NA
- Development phase
- 1,820 participants
- Enrollment target
- 1
- Study location
Study Summary
The MADIT-CRT trial is designed to determine if combined implantable cardiac defibrillator (ICD)-cardiac resynchronization therapy (CRT-D) will reduce the risk of mortality and heart failure (HF) events by approximately 25%, in subjects who are in New York Heart Association (NYHA) functional Class II with non-ischemic or ischemic cardiomyopathy and subjects who are in NYHA functional Class I with ischemic cardiomyopathy, left ventricular dysfunction (ejection fraction \[EF\] \< or = 0.30), and prolonged intraventricular conduction (QRS duration \> or = 130 ms).
Primary Outcome
MADIT-CRT was an event-driven trial in which patients were monitored for all-cause mortality and HF events. An HF event was defined as either hospitalization for symptoms and/or signs consistent with congestive HF and: 1. administration of intravenous decongestive therapy that does not involve formal in-patient hospital admission, regardless of the setting (i.e. in an emergency room setting, in the physician's office, etc.), or 2. administration of an augmented HF regimen with oral or intraveno
Conditions Studied
Interventions
- DEVICE Implantable Cardioverter Defibrillator (ICD)
- DEVICE Cardiac resynchronization therapy with defibrillation
Study Locations (1)
New York
- Multiple locations in the US and international - Rochester
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 1,820 participants |
| Start Date | 2004-12 |
| Est. Completion | 2010-09 |
| Phase | NA |
What the finished NCT00180271 record still lists
NCT00180271 is an interventional study that assigns participants to a tested intervention. Its 1,820 participants enrollment target places it among the larger protocols in the corpus, above the 294-participant average among 51 other Congestive Heart Failure trials with a reported enrollment target (519% higher).
The record links to 2 conditions, with Congestive Heart Failure appearing as the primary indexed condition, and to 2 interventions - of which Implantable Cardioverter Defibrillator (ICD) is the first listed.
NCT00180271 reports a single indexed study location in New York.
Frequently Asked Questions
What is clinical trial NCT00180271 about?
NCT00180271 is a clinical study titled "MADIT-CRT: Multicenter Automatic Defibrillator Implantation With Cardiac Resynchronization Therapy". The MADIT-CRT trial is designed to determine if combined implantable cardiac defibrillator (ICD)-cardiac resynchronization therapy (CRT-D) will reduce the risk of mortality and heart failure (HF) events by approximately 25%, in subjects who are in New York Heart Association (NYHA) functional Class I...
What is the current status of trial NCT00180271?
This trial is currently completed. It is a NA study. The enrollment target is 1,820 participants. The study started on 2004-12. Estimated completion is 2010-09.
What conditions does trial NCT00180271 study?
This clinical trial studies the following conditions: Congestive Heart Failure, Tachycardia.
What interventions are being tested in trial NCT00180271?
The interventions under investigation include: Implantable Cardioverter Defibrillator (ICD) (DEVICE), Cardiac resynchronization therapy with defibrillation (DEVICE).
Who is sponsoring clinical trial NCT00180271?
This trial is sponsored by Boston Scientific Corporation, which has 280 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT00180271 being conducted?
This trial has 1 study location across New York. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
Learn More About Clinical Trials
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Where NCT00180271's enrollment target sits among peer trials
1,820 2nd of 51 the highest of 51 other Congestive Heart Failure trials
participants (enrollment target), bucketed by value
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