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NCT00597142 · ClinicalTrials.gov registry record · Phase 4
A Prospective, Multi-center, Single Arm Study Evaluating the Express™ Renal Premounted Stent System in the Treatment of Atherosclerotic Lesions in the Aortorenal Ostium.
A Phase 4 study, sponsored by Boston Scientific Corporation.
- Completed
- Registry status
- Phase 4
- Development phase
- 100
- Enrollment target
NCT00597142: Completed Phase 4 study, sponsored by Boston Scientific Corporation.
NCT00597142 is a Phase 4 study that has completed, run by Boston Scientific Corporation. The registered enrollment target is 100 participants, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (81% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT00597142, a Phase 4 study, has completed, sponsored by Boston Scientific Corporation.
- COMPLETED
- Registry status
- Phase 4
- Development phase
- 100 participants
- Enrollment target
Study Summary
The purpose of this study is to demonstrate superior 9-month binary restenosis rate of the Express™ Renal Premounted Stent System as compared to an Objective Performance Criterion representative of PTRA, for atherosclerotic lesions in the aortorenal ostium.
Interventions
- DEVICE Express™ Renal Premounted Stent System
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 100 participants |
| Start Date | 2004-01 |
| Est. Completion | 2009-10 |
| Phase | Phase 4 |
What the finished NCT00597142 record still lists
NCT00597142 is an interventional study that assigns participants to a tested intervention. The registered 100 participants enrollment target is mid-sized for trials with a published cap, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (81% lower).
The record links to 0 conditions, and to 1 intervention - of which Express™ Renal Premounted Stent System is the first listed.
NCT00597142 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT00597142 about?
NCT00597142 is a clinical study titled "A Prospective, Multi-center, Single Arm Study Evaluating the Express™ Renal Premounted Stent System in the Treatment of Atherosclerotic Lesions in the Aortorenal Ostium.". The purpose of this study is to demonstrate superior 9-month binary restenosis rate of the Express™ Renal Premounted Stent System as compared to an Objective Performance Criterion representative of PTRA, for atherosclerotic lesions in the aortorenal ostium.
What is the current status of trial NCT00597142?
This trial is currently completed. It is a Phase 4 study. The enrollment target is 100 participants. The study started on 2004-01. Estimated completion is 2009-10.
What interventions are being tested in trial NCT00597142?
The interventions under investigation include: Express™ Renal Premounted Stent System (DEVICE).
Who is sponsoring clinical trial NCT00597142?
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 NCT00597142's enrollment target sits among peer trials
100 770th of 2000 higher than 1,148 of 2,000 other Phase 4 trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Phase 4 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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