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Study identifier: NCT07520500 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

IFOC Compared With LIFT in High Anal Fistula

Condition: Anal Fistula Surgery · High Anal Fistula  ·  Sponsor: Cairo University

PhaseNA
Planned participants66
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

Patients presenting to the outpatient clinic at Kasr Al-Ainy Hospitals with high anal fistula will be assessed according to the inclusion and exclusion criteria. The study purpose will be explained, and informed consent will be obtained from eligible participants. A detailed medical history and routine preoperative assessment will be conducted. Clinical evaluation will include identification of the internal and external openings, assessment of discharge, and continence status using the Jorge-Wexner incontinence score. MRI fistulogram will be performed preoperatively to evaluate the fistula tract and its relation to the sphincter complex. Patients will be randomly allocated into two equal groups (1:1 ratio) using a computer-generated sequence: Group A: Undergo LIFT procedure Group B: Undergo IFOC procedure Both procedures will be performed as per standard surgical techniques. Postoperatively, patients will start oral fluids after 2 hours and resume a normal diet as tolerated. Discharge is planned on the first postoperative day unless otherwise indicated. Follow-up will be conducted at 1 week, 2 weeks, 1 month, and monthly thereafter for at least 6 months to assess healing and detect complications, including recurrence.

This description comes directly from the study's public registry record.

Talk to the study team

Ahmed Mohamed Abdelaal, MD  ·  +201118732767  ·  drabdelaal90@gmail.com

Always discuss trial participation with your own doctor first.

Locations (1)

Faculty of medicine, Cairo UniversityCairo, Al-Manial, Cairo, Egypt, EgyptRecruiting

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Source record: clinicaltrials.gov/study/NCT07520500