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
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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COMPLETED
NA
86 participants
INTERVENTIONAL
2024-08-01
2025-01-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
NONE
Study Groups
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Continuous group
In this group patients under going episiotomy, went through continuous suturing
Continuous suturing
In this group, episiotomy repair was done using the continuous suturing.
Interrupted group
In this group patients under going episiotomy, went through interrupted suturing
Interrupted suturing
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.
Interrupted suturing
In this group, episiotomy repair was done using the interrupted suturing.
Eligibility Criteria
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Inclusion Criteria
* 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
* 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
20 Years
40 Years
FEMALE
No
Sponsors
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RESnTEC, Institute of Research
OTHER
Responsible Party
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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
Countries
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Other Identifiers
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DRAROOJ-SITH
Identifier Type: -
Identifier Source: org_study_id
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