Expired Study
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Detroit, Michigan 48202


Purpose:

The proposed study will investigate the efficacy of the peripheral cutting balloon (PBC) compared to the high pressure balloon in dilating venous stenosis in hemodialysis fistulas. 2. SPECIFIC AIMS Study endpoints will be: Primary Endpoint 1. Primary and assisted patency at 6 months Secondary Endpoints: 1. Procedure effectiveness/residual stenosis 2. Procedure-related complications 3. Primary patency and primary assisted patency 12 months 4. Secondary patency at 6 and 12 months 5. Number/type of secondary interventions.


Criteria:

Inclusion Criteria: - Dysfunctional fistulas will be recruited based on the presence of clinical and hemodialysis parameters Exclusion Criteria: - Arteriovenous prosthetic grafts


NCT ID:

NCT00543348


Primary Contact:

Principal Investigator
GEORGES HADDAD, MD, FACS
Henry Ford Health System


Backup Contact:

N/A


Location Contact:

Detroit, Michigan 48202
United States

GEORGES HADDAD, MD, FACS
Phone: 313-916-7308
Email: ghaddad1@hfhs.org

Site Status: Recruiting


Data Source: ClinicalTrials.gov

Date Processed: November 24, 2017

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