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NCT00643604 · ClinicalTrials.gov registry record · Phase 4
Rapid Switch From Flolan to Remodulin in the Outpatient Clinic
A Phase 4 study, sponsored by United Therapeutics.
- Terminated
- Registry status
- Phase 4
- Development phase
- 7
- Enrollment target
NCT00643604 is a Phase 4 study that was terminated before completion, run by United Therapeutics. The registered enrollment target is 7 participants.
The verdict
NCT00643604, a Phase 4 study, was terminated before completion, sponsored by United Therapeutics.
- TERMINATED
- Registry status
- Phase 4
- Development phase
- 7 participants
- Enrollment target
Study Summary
The purpose of this 8-week study is to compare the effects of switching from therapy with epoprostenol or Flolan to IV Remodulin. This study will also assess the effect that changing to Remodulin will have on patient satisfaction with their treatment and impact on quality of life.
Interventions
- DRUG treprostinil sodium
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 7 participants |
| Start Date | 2008-03 |
| Est. Completion | 2012-02 |
| Phase | Phase 4 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT00643604
The ClinicalTrials.gov registry entry for NCT00643604 describes a study currently listed as terminated, categorized as Phase 4. The registered enrollment target is 7 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is United Therapeutics, which has 63 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 1 intervention - of which treprostinil sodium is the first listed.
NCT00643604 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT00643604 about?
NCT00643604 is a clinical study titled "Rapid Switch From Flolan to Remodulin in the Outpatient Clinic". The purpose of this 8-week study is to compare the effects of switching from therapy with epoprostenol or Flolan to IV Remodulin. This study will also assess the effect that changing to Remodulin will have on patient satisfaction with their treatment and impact on quality of life.
What is the current status of trial NCT00643604?
This trial is currently terminated. It is a Phase 4 study. The enrollment target is 7 participants. The study started on 2008-03. Estimated completion is 2012-02.
What interventions are being tested in trial NCT00643604?
The interventions under investigation include: treprostinil sodium (DRUG).
Who is sponsoring clinical trial NCT00643604?
This trial is sponsored by United Therapeutics, which has 63 total clinical trials registered on ClinicalTrials.gov.
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