Skip to content

Chromic catgut versus polyglactin 910 for primary repair of episiotomy at Maitama District Hospital ,Abuja.

Chromic catgut versus polyglactin 910 for primary repair of episiotomy at Maitama District Hospital ,Abuja.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
PACTR
Registry ID
PACTR202503903855360
Enrollment
176
Registered
2025-03-10
Start date
2025-02-24
Completion date
Unknown
Last updated
2026-06-22

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

Conditions

Pregnancy and Childbirth

Interventions

chromic catgut

Sponsors

Dr Clement Mary Dennis
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: Postnatal mothers with no added risk for wound infection who have a vaginal delivery of singleton live fetus in whom a right medio-lateral episiotomy was indicated to facilitate the delivery and who are willing to participate in the study will be included

Exclusion criteria

Exclusion criteria: The exclusion criteria will include the following categories of parturient: 1. Pregnant women who decline consent to participate. 2. Women who smoke cigarettes. 3. Those who undergo instrumental vaginal delivery with forceps or ventouse. 4. Women who had a previous perineal repair of 3rd and 4th degree perineal tear. 5. Women who have extensions of lateral episiotomy. 6. Women who have Diabetes Mellitus. 7. Women who are Human immunodeficiency virus (HIV) positive. 8. Women who have primary postpartum haemorrhage (blood loss > 500mL). 9. Women who have manual removal of placenta for retained placenta. 10. Women who have perineal lesions such as warts or extensive varicose veins of the genital area.

Design outcomes

Primary

MeasureTime frame
The primary outcome measures will be wound complication rates including wound healing process, wound dehiscence and need for re-suturing, bleeding and haematoma formation, and post-operative perineal pain. The secondary outcome measures will be the severity of pain on walking, sitting, and lying posture. The wound will be assessed for pain at 24 hours, 7 days, and 6 weeks post-repair

Secondary

MeasureTime frame
secondary outcome measures will be the severity of pain on walking, sitting, and lying posture. The wound will be assessed for pain at 24 hours, 7 days, and 6 weeks post-repair

Countries

Nigeria

Contacts

Public ContactDuum Nwachukwu

Consultant OBST.AND GYNAECOLOGY

nduum@yahoo.com08033903782

Outcome results

None listed

Source: PACTR (via WHO ICTRP) · Data processed: Jun 29, 2026