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Effect of Barbed Suture and Triclosan-coated Monofilament in Emergency Surgery

NCT03763279 · Status: COMPLETED · Phase: PHASE3 · Type: INTERVENTIONAL · Enrollment: 150

Last updated 2019-09-16

No results posted yet for this study

Summary

Patients will be randomized 3 groups:

Group 1: Abdominal fascial closure will be performed with Triclosan-coated barbed Polydioxanone suture

Group 2:Abdominal fascial closure will be performed with Triclosan-coated monofilament Polydioxanone suture

Group 3: Abdominal fascial closure will be performed with monofilament Polydioxanone suture

Incisional surgical.site infection and evisceration will be recorded.

Conditions

  • Surgical Site Infection

Interventions

COMBINATION_PRODUCT

Triclosan-coated barbed suture

Use of Triclosan-coated Polydioxanone barbed suture

COMBINATION_PRODUCT

Triclosan-coated monofilament suture

Use of Triclosan-coated Polydioxanone monofilament suture

DEVICE

Monofilament suture

Use of Polydioxanone monofilament suture

Sponsors & Collaborators

  • Hospital General Universitario Elche

    lead OTHER

Principal Investigators

  • Andres Garcia-Marin · Hospital de San Juan

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2018-11-30
Primary Completion
2019-03-31
Completion
2019-03-31

Countries

  • Spain

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03763279 on ClinicalTrials.gov