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Effectiveness of Wound Drains for the Prevention Of Surgical sITe infectION

NCT05179122 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 200

Last updated 2024-02-02

No results posted yet for this study

Summary

The aim of the present randomized trial is to assess the efficacy of wound drains in terms of reducing the rates of surgical site infection in obese patients with gynecological cancer.

Conditions

  • Surgical Site Infection
  • Gynecologic Cancer
  • Wound Drain

Interventions

PROCEDURE

Surgical drain

In this arm a surgical drain will be inserted prior to surgical wound closure

Sponsors & Collaborators

  • Aristotle University Of Thessaloniki

    collaborator OTHER

  • Saint Savvas Anticancer Hospital

    collaborator OTHER

  • Metaxa Hospital

    collaborator OTHER

  • National and Kapodistrian University of Athens

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
30 Years
Max Age
85 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2021-01-01
Primary Completion
2023-12-31
Completion
2024-01-15

Countries

  • Greece

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 NCT05179122 on ClinicalTrials.gov