Evaluation of Triclosan Coated Suture in Obstetrical Surgery

Tunis University

Status and phase: Completed; Phase 4

Conditions: Cesarean Section; Infection

Treatments: Drug: Vicryl; Drug: Coated Vicryl+

Study type: Interventional

Funder types: Other

Identifiers

NCT05330650

TunisU 1

Details and patient eligibility

About

A prospective comparative randomized blinded study conducted in the obstetrics gynecology department of Ben Arous hospital over an eight-month period between November 2020 and June 2021.

The aim of this study is to evaluate effectiveness of Triclosan coated suture use in obstetrical surgery.

Enrollment: 318 patients

Sex: Female

Ages: 18+ years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• Pregnant women with indicated cesarean delivery and who have signed a written consent.

Exclusion criteria

• Cases with incomplete follow up
• Breach of operative protocol

Trial design

Primary purpose: Prevention

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Quadruple Blind

---

318 participants in 2 patient groups

Triclosan coated suture

Active Comparator group

Treatment:

Drug: Coated Vicryl+

Non coated suture

Active Comparator group

Treatment:

Drug: Vicryl