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Comparison of skin staples to subcuticular Vicryl suture for skin closure following caesarean section at the Federal Teaching Hospital Katsina

A Randomized Controlled Trial of Skin Staples Versus Subcuticular Vicryl Suture for Skin Closure Following Caesarean Section at Federal Teaching Hospital Katsina

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
PACTR
Registry ID
PACTR202412512322134
Enrollment
80
Registered
2024-12-23
Start date
2024-11-13
Completion date
Unknown
Last updated
2026-09-14

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

Conditions

caesarean section

Interventions

STUDY GROUP
Group II vicryl 20

Sponsors

Federal Teaching Hospital Katsina
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: 1. Patients of Federal Teaching Hospital, Katsina 2. Elective Caesarean section 3. Pfannenstiel or Joel Cohen skin incision 4. Gestational ages ranging from 28 weeks 0 days to 41 weeks 6 days

Exclusion criteria

Exclusion criteria: 1. Previous existing local skin infections, keloid or hypertrophied scar 2. Diabetes mellitus patients 3. Immunosuppressive disease condition, e.g. HIV infection, Systemic Lupus Erythematosus (SLE), Antiphospholipid Syndrome (APS), Multiple Sclerosis 4. Immunosuppressive treatment, e.g. prolonged use of systemic steroids >3 months 5. No consent to participate in the study

Design outcomes

Primary

MeasureTime frame
Superficial surgical site infection and postoperative wound dehiscence, defined as the observation of infection involving the skin and subcutaneous tissue of the incision site within with either purulent discharge, localized pain or tenderness, localized swelling, erythema, or heat measured using the Scar Cosmesis Assessment Rating (SCAR) scale on Day 5 and at 6 weeks post-operation

Secondary

MeasureTime frame
. Average duration of time (seconds) from the first to the last skin cut of subcuticular skin closure (control group) and from the time of first to the last skin stapler application for skin closure (study group) measured using a stop clock during the procedure ;Post-operative pain perception measured using the Numerical Pain Assessment Tool;Scar outcome measured using the Scar Cosmesis Assessment Rating (SCAR) scale ;Patient's and surgeons' satisfaction measured using the patient/surgeon scar Visual Satisfaction Scale (VSS)

Countries

Nigeria

Contacts

Public ContactHabibu Abubakar

public enquiries

abubakar.habibu@yahoo.com08035978979

Outcome results

None listed

Source: PACTR (via WHO ICTRP) · Data processed: Sep 19, 2026