Last updated: July 23, 2024
Sponsor: The Cleveland Clinic
Overall Status: Active - Recruiting
Phase
N/A
Condition
Rectal Disorders
Treatment
Ethibond suture
Vessel loop
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: 140
Treatment Group(s): 2
Primary Treatment: Ethibond suture
Phase:
Study Start date:
December 10, 2023
Estimated Completion Date:
July 31, 2025
Study Description
Connect with a study center
Cleveland Clinic Florida
Weston, Florida 33331
United StatesActive - Recruiting
Not the study for you?
Let us help you find the best match. Sign up as a volunteer and receive email notifications when clinical trials are posted in the medical category of interest to you.