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Effects of Remodulin in Patients with Critical Limb Ischemia Following a Vein Bypass Graft



Effects of Remodulin in Patients with Critical Limb Ischemia Following a Vein Bypass Graft

For Condition: Critical Limb Ischemia following Bypass Graft
Status: Recruiting
Sponsor(s): United Therapeutics ,
Synopsis: 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 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.
Details:
Eligibility:
Study Type:
  Interventional, Treatment, Randomized, Double-Blind, Placebo Control, Parallel Assignment, Safety/Efficacy Study
Minimum Age/Maximum Age: 18 Years/85 Years
Genders: Both
Protocol Entry Criteria: Patients with critical limb ischemia and an appropriate reference lower-limb ischemic wound due to documented peripheral arterial disease who have had an autogenous vein infrainguinal bypass graft performed immediately prior to study initiation.
Total Enrollment: 30

Location and Contact Information:

Vascular Institute Albany Medical College *Recruiting*
Albany,  New York,  12208
United States
Recruiting Debbie  Hill 518-262-5021

Southern Illinois University School of Medicine *Recruiting*
Springfield,  Illinois,  62702
United States
Recruiting Carol  Buettner 217-545-2320

Oregon Health Sciences University *Recruiting*
Portland,  Oregon,  97239
United States
Recruiting Rakhee  Urankar 503-494-4334

University of Massachusetts Memorial Health Center *Recruiting*
Worcester,  Massachusetts,  01655
United States
Recruiting Mary  Martella 508-856-6834


Additional Information:
Study ID Numbers:
  REM03:203; 
Study Start Date: March 2003
Record last reviewed: August 2003
Additional information available at: clinicaltrials.gov
Clinicaltrials.gov Reference link: NCT00067041

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