Blind anal fistula treatment (BAFT) for anal fistula treatment

Evaluation of blind anal fistula treatment (BAFT) for anal fistula treatment

Status

Active, not recruiting

Phases

Phase 3

Study type

Interventional

Source

IRCT

Registry ID

IRCT20190325043107N29

Enrollment

Registered

2022-04-28

Start date

2022-05-05

Completion date

Unknown

Last updated

2022-05-02

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

Conditions

Pain. Other chronic pain

Interventions

Intervention 1: Intervention group: A total of 25 patients will be included in this group after random allocation. Patients will be hospitalized and then transferred to the operating room. The BAFT me

Eligibility

Sex/Gender

All

Age

18 Years to 75 Years

Inclusion criteria

Inclusion criteria: Candidate for preanal fistula surgery

Exclusion criteria

Exclusion criteria: History of diabetes Patients with coagulation problems Patients with inflammatory bowel disease

Design outcomes

Primary

Measure	Time frame
Pain. Timepoint: Before the intervention and two weeks after the intervention. Method of measurement: Visual analog scale.	—

Secondary

Measure	Time frame
Anal fistula healing. Timepoint: Before the intervention and two weeks after the intervention. Method of measurement: Physical examination.	—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMehdi Khanbabayi Gol

Tabriz University of Medical Sciences

Khanbabayimehdi69@gmail.com+98 41 3334 7054

Outcome results

None listed

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