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NCT00231283 · ClinicalTrials.gov registry record · Phase 3
NEXUS Study for the Treatment of de Novo Native Coronary Artery Lesions
A Phase 3 study, sponsored by Cordis US.
- Completed
- Registry status
- Phase 3
- Development phase
- 100
- Enrollment target
NCT00231283: Completed Phase 3 study, sponsored by Cordis US.
NCT00231283 is a Phase 3 study that has completed, run by Cordis US. The registered enrollment target is 100 participants, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (87% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT00231283, a Phase 3 study, has completed, sponsored by Cordis US.
- COMPLETED
- Registry status
- Phase 3
- Development phase
- 100 participants
- Enrollment target
Study Summary
The objective of this study is to evaluate the effectiveness and safety of the CYPHER NxT Sirolimus-eluting Coronary Stent on the BX SONIC Over-the-Wire (OTW) Stent Delivery System (SDS) in patients with de novo native coronary artery lesions.
Primary Outcome
Procedure Success is defined as the final residual diameter stenosis \< 50 percent by Quantitative Coronary Angiography (QCA) using any percutaneous method, without the occurrence of death, Myocardial Infarction (MI), or repeat revascularization of the target lesion
Interventions
- DEVICE CYPHER NxT SES ON BX SONIC OTW STENT DELIVERY SYSTEM (SDS)
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 100 participants |
| Start Date | 2004-04 |
| Est. Completion | 2005-07 |
| Phase | Phase 3 |
What the finished NCT00231283 record still lists
NCT00231283 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 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (87% lower).
The record links to 0 conditions, and to 1 intervention - of which CYPHER NxT SES ON BX SONIC OTW STENT DELIVERY SYSTEM (SDS) is the first listed.
NCT00231283 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT00231283 about?
NCT00231283 is a clinical study titled "NEXUS Study for the Treatment of de Novo Native Coronary Artery Lesions". The objective of this study is to evaluate the effectiveness and safety of the CYPHER NxT Sirolimus-eluting Coronary Stent on the BX SONIC Over-the-Wire (OTW) Stent Delivery System (SDS) in patients with de novo native coronary artery lesions.
What is the current status of trial NCT00231283?
This trial is currently completed. It is a Phase 3 study. The enrollment target is 100 participants. The study started on 2004-04. Estimated completion is 2005-07.
What interventions are being tested in trial NCT00231283?
The interventions under investigation include: CYPHER NxT SES ON BX SONIC OTW STENT DELIVERY SYSTEM (SDS) (DEVICE).
Who is sponsoring clinical trial NCT00231283?
This trial is sponsored by Cordis US, which has 19 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT00231283's enrollment target sits among peer trials
100 1681st of 2000 higher than 288 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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