Last updated: October 16, 2025
Sponsor: The Cleveland Clinic
Overall Status: Terminated
Phase
N/A
Condition
Rectal Disorders
Treatment
Vessel loop
Ethibond suture
Clinical Study ID
NCT05933343
CCF06282023
Ages 18-70 All Genders
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
- Adult patients aged 18 years or older of either sex who present with CAF will beincluded. Both cryptoglandular fistulas and fistulas secondary to inflammatory boweldisease (IBD)
Exclusion
Exclusion Criteria:
Simple anal fistulas
Fistulas secondary to malignancy or irradiation therapy
Pregnant women
Patients with pre-existing setons
Study Design
Total Participants: 2
Treatment Group(s): 2
Primary Treatment: Vessel loop
Phase:
Study Start date:
December 10, 2023
Estimated Completion Date:
October 16, 2025
Study Description
Connect with a study center
Cleveland Clinic Florida
Weston, Florida 33331
United StatesSite Not Available
Cleveland Clinic Florida
Weston 4178003, Florida 4155751 33331
United StatesSite Not Available

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