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NCT00111488 · ClinicalTrials.gov registry record · Phase 3
Guidant Microwave Ablation System for the Treatment of Atrial Fibrillation
A Phase 3 study, sponsored by Boston Scientific Corporation.
- Terminated
- Registry status
- Phase 3
- Development phase
- 200
- Enrollment target
NCT00111488: Clinical Trial Phase 3 study, sponsored by Boston Scientific Corporation.
NCT00111488 is a Phase 3 study that was terminated before completion, run by Boston Scientific Corporation. The registered enrollment target is 200 participants, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (74% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT00111488, a Phase 3 study, was terminated before completion, sponsored by Boston Scientific Corporation.
- TERMINATED
- Registry status
- Phase 3
- Development phase
- 200 participants
- Enrollment target
Study Summary
The purpose of the Randomized Study of Surgical Ablation with Microwave Energy for the Treatment of Atrial Fibrillation (RESOLVE-AF) trial is to determine the safety and effectiveness of the Guidant FLEX® Microwave Surgical Ablation System in the treatment of permanent atrial fibrillation (AF).
Interventions
- DEVICE Flex 4 and Generator
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 200 participants |
| Start Date | 2005-06 |
| Est. Completion | 2006-12 |
| Phase | Phase 3 |
Why NCT00111488 stopped before completion
NCT00111488 is an interventional study that assigns participants to a tested intervention. The registered 200 participants enrollment target is mid-sized for trials with a published cap, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (74% lower).
The record links to 0 conditions, and to 1 intervention - of which Flex 4 and Generator is the first listed.
NCT00111488 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT00111488 about?
NCT00111488 is a clinical study titled "Guidant Microwave Ablation System for the Treatment of Atrial Fibrillation". The purpose of the Randomized Study of Surgical Ablation with Microwave Energy for the Treatment of Atrial Fibrillation (RESOLVE-AF) trial is to determine the safety and effectiveness of the Guidant FLEX® Microwave Surgical Ablation System in the treatment of permanent atrial fibrillation (AF).
What is the current status of trial NCT00111488?
This trial is currently terminated. It is a Phase 3 study. The enrollment target is 200 participants. The study started on 2005-06. Estimated completion is 2006-12.
What interventions are being tested in trial NCT00111488?
The interventions under investigation include: Flex 4 and Generator (DEVICE).
Who is sponsoring clinical trial NCT00111488?
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 NCT00111488's enrollment target sits among peer trials
200 1353rd of 2000 higher than 613 of 2,000 other Phase 3 trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Phase 3 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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