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Comparison Between Maternal Complications of Chromic Catgut and Vicryl Rapid Sutures Used for Episiotomy Repair

Comparison Between Maternal Complications of Chromic Catgut and Vicryl Rapid Sutures Used for Episiotomy Repair

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07073131
Enrollment
202
Registered
2025-07-18
Start date
2024-07-01
Completion date
2024-12-31
Last updated
2025-07-18

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

Conditions

Episiotomy Extended by Laceration, Episiotomy Wound

Keywords

Episiotomy, Pain, Wound Infection

Brief summary

Total 202 patients fulfilling the selection criteria were enrolled from labor room and underwent episiotomy. At end of procedure, females were randomly divided in two groups. In group A, females underwent suturing by using vicryl rapide. In group B, females underwent suturing by using chromic catgut. After 24 hours of delivery, females were examined for pain score. After 7 days, females were examined for wound infection, inflammation and dehiscence. All this information was recorded in proforma.

Interventions

OTHERVicryl Rapide suturing

Post episiotomy vicryl rapide suturing material is used for stitching episiotomy laceration.

OTHERChromic catgut suturing

Post episiotomy chromic catgut suturing material is used for stitching episiotomy laceration

Sponsors

Huma Ijaz
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 35 Years
Healthy volunteers
Yes

Inclusion criteria

* Primigravida of age 18-35 years * Gestational age during 37-40 weeks

Exclusion criteria

* Females with abnormal placenta, non-cephalic presentation, multiple fetus, premature rupture of membranes, unclean vaginal examination. * pre-delivery hemoglobin \<9 g/dl, * Manual removal of placenta * Vulvar hematoma and vaginal tears

Design outcomes

Primary

MeasureTime frameDescription
Wound dehiscence7 daysWound dehiscence was labeled if there was partial or total separation of previously approximated wound edges, due to a failure of proper wound healing within 7 days of episiotomy.
Post surgical pain7 daysAfter 24 hours of episiotomy participants were examined for pain score by using visual analogue scale.
Wound Infection7 daysWound infection was labeled if participant developed pain and pus discharge at wound site, along with fever (\>100F) within 7 days of episiotomy.

Countries

Pakistan

Outcome results

None listed

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