Aggrenox Prevention of Access Stenosis

NCT00067119 · Status: COMPLETED · Phase: PHASE3 · Type: INTERVENTIONAL · Enrollment: 649

Last updated 2017-09-19

No results posted yet for this study

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

Placebo

Sponsors & Collaborators

  • The Cleveland Clinic

    collaborator OTHER
  • Boston University

    collaborator OTHER
  • Duke University

    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

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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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00067119 on ClinicalTrials.gov