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NCT00947310 · ClinicalTrials.gov registry record · NA
Multicenter Automatic Defibrillator Implantation Trial - Reduce Inappropriate Therapy
A NA study, sponsored by Boston Scientific Corporation.
- Completed
- Registry status
- NA
- Development phase
- 1,500
- Enrollment target
NCT00947310: Completed NA study, sponsored by Boston Scientific Corporation.
NCT00947310 is a NA study that has completed, run by Boston Scientific Corporation. The registered enrollment target is 1,500 participants, roughly in line with the 1,404-participant average among 58,714 other NA trials with a reported enrollment target. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT00947310, a NA study, has completed, sponsored by Boston Scientific Corporation.
- COMPLETED
- Registry status
- NA
- Development phase
- 1,500 participants
- Enrollment target
Study Summary
This study will assess the impact of higher rate cutoffs and longer delays than standard programming on inappropriate therapy in primary prevention ICD and CRT-D patients.
Primary Outcome
First occurance of inappropriate therapy (either anti-tachycardia pacing or shock)
Interventions
- DEVICE Standard ICD programming
- DEVICE High rate cutoff
- DEVICE Long delay
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 1,500 participants |
| Start Date | 2009-09 |
| Est. Completion | 2012-12 |
| Phase | NA |
What the finished NCT00947310 record still lists
NCT00947310 is an interventional study that assigns participants to a tested intervention. Its 1,500 participants enrollment target places it among the larger protocols in the corpus, roughly in line with the 1,404-participant average among 58,714 other NA trials with a reported enrollment target.
The record links to 0 conditions, and to 3 interventions - of which Standard ICD programming is the first listed.
NCT00947310 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT00947310 about?
NCT00947310 is a clinical study titled "Multicenter Automatic Defibrillator Implantation Trial - Reduce Inappropriate Therapy". This study will assess the impact of higher rate cutoffs and longer delays than standard programming on inappropriate therapy in primary prevention ICD and CRT-D patients.
What is the current status of trial NCT00947310?
This trial is currently completed. It is a NA study. The enrollment target is 1,500 participants. The study started on 2009-09. Estimated completion is 2012-12.
What interventions are being tested in trial NCT00947310?
The interventions under investigation include: Standard ICD programming (DEVICE), High rate cutoff (DEVICE), Long delay (DEVICE).
Who is sponsoring clinical trial NCT00947310?
This trial is sponsored by Boston Scientific Corporation, which has 280 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT00947310's enrollment target sits among peer trials
1,500 65th of 2000 higher than 1,933 of 2,000 other NA trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other NA 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
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