Actively Recruiting

Phase Not Applicable
Age: 20Years - 65Years
All Genders
NCT07399353

Comparative Study: Fistula Rerouting vs. LIFT for High Perianal Fistula

Led by Cairo University · Updated on 2026-02-10

40

Participants Needed

1

Research Sites

39 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The goal of this clinical trial is to compare two different surgery methods for treating a complex type of anal fistula. This condition is an abnormal tunnel connecting the inside of the anus to the skin nearby. The main questions the study aims to answer are: Which surgery has a lower chance of the fistula coming back (recurrence)? Which surgery has a lower chance of causing problems with bowel control (incontinence) after healing? Researchers will compare two surgery groups: Group 1: Fistula Rerouting Technique - a two-step surgery that moves the fistula tract to a safer area before opening it. Group 2: LIFT Technique - a surgery that ties off and closes the fistula tract from between the anal muscles. Participants will be randomly assigned by a computer to one of these two surgery groups. This helps ensure the comparison between the two surgeries is fair. Participants in this study will: * Have tests before surgery, including an MRI scan, to confirm they have the specific type of fistula being studied. * Undergo one of the two planned surgical procedures. * Attend follow-up visits after surgery at 1 week, 2 weeks, 1 month, and 3 months. * Be checked during these visits for wound healing, pain, infection, and bowel control. * Have another MRI scan if the fistula is suspected to have come back.

CONDITIONS

Official Title

Comparative Study: Fistula Rerouting vs. LIFT for High Perianal Fistula

Who Can Participate

Age: 20Years - 65Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Adult patients aged 20 to 65 years with high perianal fistula, defined as trans-sphincteric fistula traversing the upper two-thirds of the external anal sphincter or extrasphincteric fistula
  • Patients with recurrent perianal fistula
  • Ability to provide informed consent
Not Eligible

You will not qualify if you...

  • Preoperative fecal incontinence as assessed by the Cleveland Clinic Fecal Incontinence Score
  • Diagnosis of inflammatory bowel disease such as Crohn's disease or ulcerative colitis
  • Pregnant women
  • Pediatric patients under 20 years old
  • Patients with complex, branching fistula tracts
  • Contraindication to spinal or general anesthesia or surgery

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Faculty of Medicine Cairo University

Cairo, Al-Manial Cairo, Egypt, 11956

Actively Recruiting

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Research Team

M

Mostafa Mohamed Sedky, Lecturer

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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