Clinical trial

Study of Remodulin in Patients With Critical Limb Ischemia With No Planned…

NCT00060996 · United Therapeutics, Industry · Terminated

Key facts

NCT number NCT00060996
Title Study of Remodulin in Patients With Critical Limb Ischemia With No Planned Revascularization Procedures
Official title A Randomized Placebo-Controlled, 12-Week Multicenter Study of the Safety and Efficacy of Continuous or Daily Administration of Remodulin® (Treprostinil Sodium) Injection in Patients With CLI With No Planned Revascularization Procedures
Lead sponsor United Therapeutics, Industry
Status Terminated
Phase Phase 3
Study type Interventional
Conditions Critical Limb Ischemia, Peripheral Vascular Disease, Foot Ulcers, Rest Leg Pain
Intervention type Drug
Interventions Remodulin® (treprostinil sodium) Injection
Enrollment 30
Start date Feb 1, 2003
Primary completion Sep 1, 2004
Completion Sep 1, 2004
First posted May 20, 2003
Last update posted Mar 7, 2013
Countries United States

At a glance

  • 1–9 Study sites
  • No Results posted
  • None Linked FDA submissions

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

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Source: U.S. National Library of Medicine (NLM), ClinicalTrials.gov · Source date:

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