search
Back to results

Study of Remodulin in Patients With Critical Limb Ischemia With No Planned Revascularization Procedures

Primary Purpose

Critical Limb Ischemia, Peripheral Vascular Disease, Foot Ulcers

Status
Terminated
Phase
Phase 3
Locations
United States
Study Type
Interventional
Intervention
Remodulin® (treprostinil sodium) Injection
Sponsored by
United Therapeutics
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional treatment trial for Critical Limb Ischemia focused on measuring Critical Limb Ischemia, Peripheral Vascular Disease, UT-15, Remodulin, treprostinil

Eligibility Criteria

18 Years - 85 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Patients with Stage III or IV critical limb ischemia due to documented peripheral arterial disease with no planned interventional vascular procedures

Sites / Locations

  • University of South Florida College of Medicine
  • University of Massachusetts Memorial Health
  • Minneapolis Heart Institute
  • Oregon Health Sciences University
  • Presbyterian Medical Center, Philadelphia Heart Institute
  • South Carolina Heart Center
  • The Methodist Hospital

Outcomes

Primary Outcome Measures

Secondary Outcome Measures

Full Information

First Posted
May 19, 2003
Last Updated
March 5, 2013
Sponsor
United Therapeutics
search

1. Study Identification

Unique Protocol Identification Number
NCT00060996
Brief 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
Study Type
Interventional

2. Study Status

Record Verification Date
March 2013
Overall Recruitment Status
Terminated
Study Start Date
February 2003 (undefined)
Primary Completion Date
September 2004 (Actual)
Study Completion Date
September 2004 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
United Therapeutics

4. Oversight

5. Study Description

Brief Summary
The purpose of this study is to assess and compare the safety of continuous and daily subcutaneous Remodulin therapy in patients with critical limb ischemia (CLI) with no planned vascular interventional procedures; and to determine the effect of Remodulin on wound healing and treadmill walk distance.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Critical Limb Ischemia, Peripheral Vascular Disease, Foot Ulcers, Rest Leg Pain
Keywords
Critical Limb Ischemia, Peripheral Vascular Disease, UT-15, Remodulin, treprostinil

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
Double
Allocation
Randomized
Enrollment
30 (false)

8. Arms, Groups, and Interventions

Intervention Type
Drug
Intervention Name(s)
Remodulin® (treprostinil sodium) Injection

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
85 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Patients with Stage III or IV critical limb ischemia due to documented peripheral arterial disease with no planned interventional vascular procedures
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Michael Wade, PhD
Organizational Affiliation
United Therapeutics
Official's Role
Study Director
Facility Information:
Facility Name
University of South Florida College of Medicine
City
Tampa
State/Province
Florida
ZIP/Postal Code
33606
Country
United States
Facility Name
University of Massachusetts Memorial Health
City
Worcester
State/Province
Massachusetts
ZIP/Postal Code
01655
Country
United States
Facility Name
Minneapolis Heart Institute
City
Minneapolis
State/Province
Minnesota
ZIP/Postal Code
55407-1139
Country
United States
Facility Name
Oregon Health Sciences University
City
Portland
State/Province
Oregon
ZIP/Postal Code
97239
Country
United States
Facility Name
Presbyterian Medical Center, Philadelphia Heart Institute
City
Philadelphia
State/Province
Pennsylvania
ZIP/Postal Code
19104
Country
United States
Facility Name
South Carolina Heart Center
City
Columbia
State/Province
South Carolina
ZIP/Postal Code
29204
Country
United States
Facility Name
The Methodist Hospital
City
Houston
State/Province
Texas
ZIP/Postal Code
77030
Country
United States

12. IPD Sharing Statement

Learn more about this trial

Study of Remodulin in Patients With Critical Limb Ischemia With No Planned Revascularization Procedures

We'll reach out to this number within 24 hrs