High Type Fistula in Ano, Use Staged Seton, Loose Thick Sutures

NCT05223309 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 100

Last updated 2022-02-03

No results posted yet for this study

Summary

Fistula in ano is a chronic problem for the patients. It causes distressing because of foul odor and soiling with recurrent infection and discharge. Recurrence and anal sphincter injury were the most critical complications following surgery. Loose, thick Seton placement was the most promising surgical operation. To reduce the time of Seton placement, therefore, decreasing the suffering of patients from soiling and multiple dressing.

Conditions

  • Fistula in Ano

Interventions

OTHER

Usinf thick loose sutures in seton techingues

All patients were informed about doing fistulectomy and thick silk Seton suture placement for three months by excising the extrasphincteric part and putting the Seton suture to the intersphincteric part. Then, the second stage of operation includes the excision of the changing low type tract in which the silk Seton placed. We decrease the time of Seton placement in this study for three months to reduce the annoying symptoms of the patients. Therefore, the patient admitted to the operation theater after obtaining written consent. Most of the patients anesthetized by spinal anesthesia. In the operation theater, the patient assumed a lithotomy position . After that, the injection of a solution, which is a mixture of methylene blue dye and hydrogen peroxide into the external opening of the fistula, was done to find the internal opening. The exit of color dye or bubbles achieved to localized of inner opening from it after using intraoperative proctoscopy examination.

Sponsors & Collaborators

  • Jabir Ibn Hayyan Medical University

    lead OTHER

Principal Investigators

  • Samer Al-Hakkak, Ph.D. · Jabir Ibn Hayyan Medical University

Eligibility

Min Age
20 Years
Max Age
60 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2018-02-20
Primary Completion
2019-03-12
Completion
2021-01-25

Countries

  • Iraq

Study Locations

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Read the full study record

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View NCT05223309 on ClinicalTrials.gov