Ireland
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Recruiting Not applicable

IFOC Compared With LIFT in High Anal Fistula

NCT07520500 · tracked via the Priya Life Science Egypt tracker
Phase
Not applicable
Started
2026-04-19
Last updated
2026-05-22

Condition(s) studied

Anal Fistula SurgeryHigh Anal Fistula

Investigational drug(s) / intervention(s)

Intra-anal Fistulotomy With Fistula Opening Closure (IFOC)Ligation of the Intersphincteric Fistula Tract (LIFT)

Intra-anal Fistulotomy With Fistula Opening Closure (IFOC): The fistulous tract was identified using an arterial clamp and confirmed by water injection. Intra-anal fistulotomy was performed with electrocautery, followed by curettage of granulation tissue. The internal opening was closed with absorbable sutures in a horizontal mattress fashion, with closure confirmed by water injection. The external tract was further curetted, a tube drain was inserted, and reinforcing sutures were applied to promote healing.

Ligation of the Intersphincteric Fistula Tract (LIFT): The internal opening was identified by injection through the external opening. The tract was dissected in the intersphincteric plane, ligated at two points, and divided. Closure was confirmed by reinjection, the external opening was curetted and drained, and the incision was loosely closed.

Study summary

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.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Patients with high anal fistula from both gender Exclusion Criteria: * Patient with preoperative fecal incontinence * Fistula secondary to colorectal malignancy * Patients with inflammatory bowel disease * Fistula secondary to trauma or radiation * Low anal fistula

Primary outcome measure(s)

  • Assessment of failure rate of IFOC and LIFT procedures — Up to 6 months postoperatively
    Assessment of failure rate, defined as failure of healing or recurrence of anal fistula during the follow-up period, in both treatment groups. (Healing is defined as: Complete closure of the external opening, Absence of pus discharge , Absence of local pain or inflammation and No detectable tract on examination ) (Recurrence is defined as: Reappearance of discharge from the previous external opening after initial healing, or development of a new fistulous opening at or near the surgical site.)

Trial sites (1)

FacilityCityRegionStatus
Faculty of medicine, Cairo University Cairo Al-Manial, Cairo, Egypt Recruiting

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07520500 on ClinicalTrials.gov ↗ ← All trials in Egypt