Investigating the effect of using silver nitrate and platelet fibrin glue in the treatment of anal fistulas

Phase 2

• Conditions: Anal fistula.; Anal fistula; K60.3

• Registration Number: IRCT20191228045924N4
• Lead Sponsor: Mashhad University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 3 April 2023

Recruitment & Eligibility

• Status: Pending
• Sex: All
• Target Recruitment: 10

Inclusion Criteria

Patients who have a perianal fistula resistant to surgical treatment as diagnosed by a medical specialist
Patients should be over 18 years old
Obtain written consent

Exclusion Criteria

Patients who, in addition to anal fistula, have other urinary fistulas/active infection/carcinoma in situ/tumor.

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Discharge amount. Timepoint: Before the intervention and after the intervention every 24 hours. Method of measurement: By visual observation of the dressing that is placed on the fistula site.;The duration of recovery, which is the number of days it takes for the discharge from the fistula to stop. Timepoint: Every 24 hours (every day). Method of measurement: By visual observation of the dressing that is placed on the fistula site.;Presence of inflammation and infection. Timepoint: Before the intervention and after the intervention every week for one month. Method of measurement: Clinical examination.

Secondary Outcome Measures

Name	Time	Method
Reepithelialisation and fistula closure. Timepoint: During the 6-month follow-up period of the patient. Method of measurement: clinical examination.