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

To Compare the Frequency of Post-operative Pain of Continuous Versus Interrupted Suturing Technique in Episiotomy

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07050615
Enrollment
86
Registered
2025-07-03
Start date
2024-08-01
Completion date
2025-01-31
Last updated
2025-07-03

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

Conditions

Post Operative Pain

Brief summary

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

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.

Interventions

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

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

Sponsors

RESnTEC, Institute of Research
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
20 Years to 40 Years
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frameDescription
Post operative pain48 hoursPost-operative pain (yes/no) was noted using the visual analogue scale (VAS).

Countries

Pakistan

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026