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NCT00067041 · ClinicalTrials.gov registry record · Phase 2
Effects of Remodulin in Patients With Critical Limb Ischemia Following a Vein Bypass Graft
A Phase 2 study, sponsored by United Therapeutics.
- Terminated
- Registry status
- Phase 2
- Development phase
- 30
- Enrollment target
NCT00067041: Clinical Trial Phase 2 study, sponsored by United Therapeutics.
NCT00067041 is a Phase 2 study that was terminated before completion, run by United Therapeutics. The registered enrollment target is 30 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (77% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT00067041, a Phase 2 study, was terminated before completion, sponsored by United Therapeutics.
- TERMINATED
- Registry status
- Phase 2
- Development phase
- 30 participants
- Enrollment target
Study Summary
Approximately 30 patients will be enrolled in this 12-week study designed to assess the effect of continuous subcutaneous Remodulin therapy on the outcome of infrainguinal bypass grafts in patients with critical limb ischemia (CLI). Portions of the study will be conducted in the hospital and on an out-patient basis. The study will be conducted at multiple centers.
Interventions
- DRUG Remodulin (treprostinil sodium) Injection
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 30 participants |
| Start Date | 2003-03 |
| Est. Completion | 2003-12 |
| Phase | Phase 2 |
Why NCT00067041 stopped before completion
NCT00067041 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 30 participants, a relatively small participant target, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (77% lower).
The record links to 0 conditions, and to 1 intervention - of which Remodulin (treprostinil sodium) Injection is the first listed.
NCT00067041 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT00067041 about?
NCT00067041 is a clinical study titled "Effects of Remodulin in Patients With Critical Limb Ischemia Following a Vein Bypass Graft". Approximately 30 patients will be enrolled in this 12-week study designed to assess the effect of continuous subcutaneous Remodulin therapy on the outcome of infrainguinal bypass grafts in patients with critical limb ischemia (CLI). Portions of the study will be conducted in the hospital and on an o...
What is the current status of trial NCT00067041?
This trial is currently terminated. It is a Phase 2 study. The enrollment target is 30 participants. The study started on 2003-03. Estimated completion is 2003-12.
What interventions are being tested in trial NCT00067041?
The interventions under investigation include: Remodulin (treprostinil sodium) Injection (DRUG).
Who is sponsoring clinical trial NCT00067041?
This trial is sponsored by United Therapeutics, which has 63 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT00067041's enrollment target sits among peer trials
30 1582nd of 2000 higher than 332 of 2,000 other Phase 2 trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Phase 2 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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