Aggrenox Prevention of Access Stenosis
NCT00067119 · Status: COMPLETED · Phase: PHASE3 · Type: INTERVENTIONAL · Enrollment: 649
Last updated 2017-09-19
Summary
The objective of the study is to determine whether Aggrenox (Boehringer-Ingelheim) prolongs primary unassisted patency in newly created arteriovenous grafts. This record previously included information for both the GRAFT and FISTULA trials.
Conditions
Interventions
- DRUG
-
Aggrenox
- DRUG
Sponsors & Collaborators
-
The Cleveland Clinic
collaborator OTHER -
Boston University
collaborator OTHER - collaborator OTHER
-
University of Iowa
collaborator OTHER -
MaineHealth
collaborator OTHER -
University of Texas Southwestern Medical Center
collaborator OTHER -
University of Alabama at Birmingham
collaborator OTHER -
Washington University School of Medicine
collaborator OTHER -
Baystate Medical Center
collaborator OTHER -
Vanderbilt University
collaborator OTHER -
CAMC Health System
collaborator OTHER -
Emory University
collaborator OTHER -
St. Louis University
collaborator OTHER -
Tyler Nephrology Associates
collaborator UNKNOWN -
Vascular Surgery Associates LLC
collaborator OTHER -
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
lead NIH
Principal Investigators
-
John W Kusek, Ph.D. · NIDDK - Telephone: 301-594-7717; Email: [email protected]
-
Catherine Meyers, M.D. · NIDDK - Telephone: 301-451-4901; Email: [email protected]
Study Design
- Allocation
- RANDOMIZED
- Purpose
- PREVENTION
- Masking
- QUADRUPLE
- Model
- PARALLEL
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2003-01-01
- Primary Completion
- 2008-01-31
- Completion
- 2008-01-31
- FDA Drug
- Yes
Countries
- United States
Study Locations
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