N/A
Completed N=408
Multicenter Automatic Defibrillator Implantation Trial With Cardiac Resynchronization Therapy Post Approval Registry
Source: ClinicalTrials.gov NCT01294449 ↗Enrolled (actual)
408
Serious AEs
38.3%
Results posted
Dec 2014
Primary outcomePrimary: All-Cause Mortality — 11; 12 participants — p=0.370
Summary
MADIT-CRT PAR is an FDA mandated follow-up registry for patients that participated in the MADIT-CRT IDE study examining long-term mortality.
(MADIT-CRT IDE: NCT00180271)
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY All-Cause Mortality |
11; 12 | 0.370 |
Eligibility Criteria
Inclusion Criteria
- Active patients who were enrolled in the MADIT-CRT IDE (NCT00180271)within the United States
Exclusion Criteria
- Patients who are unable or unwilling to comply with the protocol requirements
Data sourced from ClinicalTrials.gov (NCT01294449). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication. Informational only — not medical advice.