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Comparison of the two methids of conventional internal partial sphincterotomy and tailored sphincterotomy of string suture anoscope in chronic anal fissure surgery

Comparison of the results of chronic anal fissure surgery between conventional internal partial sphincterotomy and tailored sphincterotomy of string suture anoscope

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20210919052515N6
Enrollment
60
Registered
2025-06-20
Start date
2025-07-23
Completion date
Unknown
Last updated
2025-07-21

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Chronic anal fissure. Chronic anal fissure

Interventions

Intervention 1: Intervention group: In tailored Sphincterotomy group , a No. 34 purse-string anoscope will be inserted and rotated circumferentially. Any areas of tightness will be incised using elect

Sponsors

Oroumia University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: Age between 18-65 old years Chronic anal fissure lasting more than one month Exhibiting signs of chronicity upon anal examination such as the presence of a skin tag Vsible fibers of the internal anal sphincter at the base of the wound

Exclusion criteria

Exclusion criteria: Patients with acute fissures Coexicted fissure with fistula or inflammatory bowel disease A history of systemic diseases A history of anal surgery (for fissure, fistula, or hemorrhoids) Fecal incontinence Perineal tears following delivery Prior radiotherapy Use of corticosteroids or other immunosuppressive drugs pregnant women

Design outcomes

Primary

MeasureTime frame
Complete treatment of Fischer. Timepoint: Weeks one, four, eight, and 6 months after surgery. Method of measurement: Clinical examination.;Gas incontinence. Timepoint: Weeks one, four, eight, and 6 months after surgery. Method of measurement: Questioning the patient.;Fecal incontinence. Timepoint: Weeks one, four, eight, and 6 months after surgery. Method of measurement: Questioning the patient.

Secondary

MeasureTime frame
Pain score. Timepoint: After surgery during recovery. Method of measurement: Visual Analogue Scale (VAS).;Dosage of analgesia. Timepoint: 24 hours after surgery. Method of measurement: Milligram.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr. Naser Masoudi

Oroumia University of Medical Sciences

masoudi.n@umsu.ac.ir+98 44 3345 7286

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026