Comparison of the Frequency of Post-Operative Pain of Continuous Versus Interrupted Suturing Techniques in Episiotomy

NCT ID: NCT07050615

Last Updated: 2025-07-03

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

86 participants

Study Classification

INTERVENTIONAL

Study Start Date

2024-08-01

Study Completion Date

2025-01-31

Brief Summary

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Post-operative pain is the most prevalent issue following an episiotomy, greatly affecting patients both physically and mentally, resulting in increased morbidity. This study seeks to compare the effectiveness of continuous and interrupted suturing techniques for episiotomy post-operative pain among the local population.

Detailed Description

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There is a lack of recent local data regarding the management of post-operative pain using different suturing techniques. The findings of this study would help in adopting a more effective technique, resulting in reducing the postoperative pain and lowering morbidity. Practical recommendations can be made to enhance routine practices and establish guidelines for these patients.

Conditions

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Post Operative Pain

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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Continuous group

In this group patients under going episiotomy, went through continuous suturing

Group Type EXPERIMENTAL

Continuous suturing

Intervention Type PROCEDURE

In this group, episiotomy repair was done using the continuous suturing.

Interrupted group

In this group patients under going episiotomy, went through interrupted suturing

Group Type EXPERIMENTAL

Interrupted suturing

Intervention Type PROCEDURE

In this group, episiotomy repair was done using the interrupted suturing.

Interventions

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Continuous suturing

In this group, episiotomy repair was done using the continuous suturing.

Intervention Type PROCEDURE

Interrupted suturing

In this group, episiotomy repair was done using the interrupted suturing.

Intervention Type PROCEDURE

Eligibility Criteria

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Inclusion Criteria

* Pregnant females
* Aged 20-40years
* Undergoing an episiotomy to facilitate the delivery of the head in the labor room
* First or second pregnancy
* Gestational age of 37-41+6 weeks

Exclusion Criteria

* Females, undergone an instrumental vaginal delivery
* With a history of previous perineal surgery
* With high-risk pregnancies (those having hypertension, anemia or bleeding tendency, diabetes mellitus, a suspected genital infection)
* With impaired immunity
* Taking corticosteroids
Minimum Eligible Age

20 Years

Maximum Eligible Age

40 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

No

Sponsors

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RESnTEC, Institute of Research

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Arooj Akram

Role: PRINCIPAL_INVESTIGATOR

Shahida Islam Medical Complex, Lodhran

Joveria Sadaf

Role: PRINCIPAL_INVESTIGATOR

Shahida Islam Medical Complex, Lodhran

Locations

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Shahida Islam Medical Complex

Lodhran, Punjab Province, Pakistan

Site Status

Countries

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Pakistan

Other Identifiers

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DRAROOJ-SITH

Identifier Type: -

Identifier Source: org_study_id

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