Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

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.

View on ClinicalTrials.gov ↗

View your shortlist →

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

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

FieldValue
Enrollment Target 1,820 participants
Start Date 2004-12
Est. Completion 2010-09
Phase NA
Boston Scientific Corporation

280 total trials

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.

Similar trials for Congestive Heart Failure

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

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

Each bar is a band; taller bars hold more other Congestive Heart Failure trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT05897788 · 1,808 participants · NA

    Text-Messaging Telehealth and Contingency Management for Opioid Use Disorder Treatment Engagement

  • NCT05935007 · 1,805 participants

    Aveir DR Real-World Evidence Post-Approval Study

  • NCT07104240 · 1,836 participants · NA

    A Vaccine Promotion Package (TweenVax) to Improve Adolescent HPV Vaccination, TweenVax Trial

  • NCT06740630 · 1,840 participants · Phase 3

    A Study on the Immune Response and Safety of an Investigational Chickenpox Vaccine When Given to Healthy Children 12 to 15 Months of Age

Similar registry start date

  • NCT05988463 · started 2027-01-01 · Phase 1

    Dose-Escalation Study of Artesunate Patients With IPF

  • NCT07219706 · started 2026-12-10 · NA

    Dietary Fiber and Time Restricted Eating

  • NCT02831335 · started 2026-12-01

    Technical Development of Multi-Parametric Renocerebral MRI

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

Source: ClinicalTrials.gov NCT00180271, the US trial registry maintained by the National Library of Medicine. NCT00180271 (large enrollment · single site footprint · completed) retrieved and formatted by PlainTrial, see methodology.