Surgical glue may boost healing for tough anal fistulas
NCT ID NCT07676825
First seen Jun 30, 2026 · Last updated Jul 01, 2026 · Updated 1 time
Summary
This study compares a standard seton (a thread used to drain and heal fistulas) with one coated in Glubran, a surgical glue with antimicrobial and healing properties. The trial includes adults with high or complex anal fistulas, a painful condition that can cause infection and incontinence. Researchers will track healing time, pain, continence, and complications over six months to see if the glue-coated seton leads to better outcomes.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Glubran (surgical glue) coated seton
- What this could lead to
- If successful, this could offer a better healing option for complex anal fistulas with less pain and fewer complications.
- What could go wrong
- This is a small, early-stage trial with only 36 participants, so results may not apply broadly. The glue could cause irritation or fail to improve outcomes.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
-
Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
-
36 people
The number who actually took part.
- Started
-
Jan 2026
- Expected to finish
-
Jul 2026
An estimate. End dates often move.
- Lead sponsor
-
Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
-
18 years and older
- Sex
-
Anyone
- Healthy volunteers
-
Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: - Patients diagnosed with high trans-sphincteric/Extrasphinteric/supra-sphincteric/complex Fistula confirmed clinically and MRI Fistulogram * Age ≥ 18 years * Patients fit for surgery. Exclusion Criteria: * Patients with Crohn's disease, tuberculosis, malignancy, or radiation-associated fistulas (due to different healing patterns and management protocols). * Presence of acute perianal abscess at the time of surgery * Patients with uncontrolled comorbidities (e.g., diabetes mellitus, bleeding disorders, immunosuppression) that could affect healing.
Get updates
Get notified about this study
Sign up to get updates when this study changes or when new studies for Perianal fistula are added.
Genom att skicka in godkänner du våra Användarvillkor
Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
-
Kasr Al Ainy Hospital
Giza, Giza Governorate, 11562, Egypt
More trials for these conditions
Other studies related to the condition(s) this trial covers.
- Laser and the Body's own healing factors tested against stubborn anal fistulas
- Can a laser seal fistulas without major surgery?
- Can a drug plus surgery heal Crohn's fistulas for good?
- Can stem cell vesicles heal Crohn's fistulas?
- Laser vs. scalpel: which heals anal fistula faster?
- Anal fistula surgery showdown: which technique spares continence?