Comparison of Prolene Thread Seton Vs Silk Thread Seton for the Treatment of Perianal Fistula

NCT ID: NCT03763981

Last Updated: 2018-12-04

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

100 participants

Study Classification

INTERVENTIONAL

Study Start Date

2017-09-01

Study Completion Date

2018-08-30

Brief Summary

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It is a randomized control trial in which we will treat the patients with perianal fistula with seton placement. We will divide the patients in two groups. Group I will be treated with silk seton and Group II will be treated with prolene setone. The outcome will be then followed as fistula healing and recurrence.

Detailed Description

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Conditions

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Perianal Fistula

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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prolene seton

Prolene thread will be used as seton treatment for perianal fistulas

Group Type ACTIVE_COMPARATOR

prolene seton treatment

Intervention Type PROCEDURE

patients with perianal fistulas will treated with seton placement by prolene thread

silk seton

Silk thread will be used as seton treatment for perianal fistulas

Group Type ACTIVE_COMPARATOR

silk seton treatment

Intervention Type PROCEDURE

patients with perianal fistulas will treated with seton placement by silk thread

Interventions

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prolene seton treatment

patients with perianal fistulas will treated with seton placement by prolene thread

Intervention Type PROCEDURE

silk seton treatment

patients with perianal fistulas will treated with seton placement by silk thread

Intervention Type PROCEDURE

Eligibility Criteria

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Inclusion Criteria

* Patients of both sexes and aged 20 years and above with high perianal fistula

Exclusion Criteria

* Low perianal fistulas Fistulas due to chrons disease, TB or carcinoma
Minimum Eligible Age

20 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Services Hospital, Lahore

OTHER_GOV

Sponsor Role lead

Responsible Party

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Dr. SamiUllah

principal investigator

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Mahmmood Ayyaz, mbbs, fcps

Role: STUDY_DIRECTOR

Services Hospital, Lahore

Locations

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Services hospital

Lahore, Punjab Province, Pakistan

Site Status

Countries

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Pakistan

Other Identifiers

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s5

Identifier Type: -

Identifier Source: org_study_id

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