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A clinical trial to study the effect of two procedures, Surgical Bundle with Preoperative Skin Preparation and Vaginal Cleaning and Surgical Bundle without Preoperative Skin Preparation and Vaginal Cleaning on Prevention of Surgical Site Infections in women undergoing Caesarean Section

Effect of Surgical Bundle with Preoperative Skin Preparation and Vaginal Cleaning versus Surgical Bundle without Preoperative Skin Preparation and Vaginal Cleaning on Prevention of Surgical Site Infections in women undergoing Caesarean Section- A Randomised Controlled Trial - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/02/080629
Enrollment
170
Registered
2025-02-14
Start date
Unknown
Completion date
Unknown
Last updated
2025-03-03

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

Conditions

Health Condition 1: O94- Sequelae of complication of pregnancy, childbirth, and the puerperium

Interventions

Intervention1: Surgical bundle with preoperative skin preparation and vaginal cleaning: Vaginal cleaning will be done using chlorhexidine 0.25% solution. Skin preparation will be done using 0.25% chlo

Sponsors

NKP Salve Institute of Medical Sciences and Research Centre and Lata Mangeshkar Hospital
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients undergoing caesarean section both elective and emergency. The patient who has given consent for the study.

Exclusion criteria

Exclusion criteria: Patients with comorbidities like Diabetes Mellitus. Patients with a body mass index of more than 30 kilograms per meter square. Patients with Premature Rupture of membranes for more than 18 hours. Patients with severe anemia with hemoglobin less than 7 grams per decilitre. Patient with recent infections at the site of the incision before caesarean section. Patients already suffering from fever.

Design outcomes

Primary

MeasureTime frame
Suture Site ExaminationTimepoint: Day 2, day 4, and day 9 post-operatively.—

Secondary

MeasureTime frame
NilTimepoint: Nil—

Countries

India

Contacts

Public ContactDr Savita Somalwar

NKP Salve Institute of Medical Sciences and Research Centre and Lata Mangeshkar Hospital

somalwar.sa@gmail.com9158920941

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026