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Comparison Of Suture Materials on Sectio Scars (COSMOSS)

NCT05096910 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 100

Last updated 2021-10-27

No results posted yet for this study

Summary

This multicenter prospective randomized controlled trial aims to investigate the ishtmocele rates after c-section delivery depending on using different suture materials for the uterine closure.

Conditions

  • Uterine Scar

Interventions

PROCEDURE

Uterine Closure with monofilament or polyfilament suture materials

Postoperative 6th-month isthmocele rates

Sponsors & Collaborators

  • Bursa Medicana Hospital

    collaborator UNKNOWN

  • UMI Health Center

    collaborator UNKNOWN

  • Ceylan Hospital

    collaborator UNKNOWN

  • Uludag University

    lead OTHER

Principal Investigators

  • Gurkan Uncu, Prof. · Bursa Uludag University Faculty of Medicine

Study Design

Allocation
RANDOMIZED
Purpose
DIAGNOSTIC
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
40 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2020-09-04
Primary Completion
2022-01-01
Completion
2022-01-01

Countries

  • Turkey (Türkiye)

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 NCT05096910 on ClinicalTrials.gov