The Effect of Suture Materials With Different Absorption NCT04455321

Updated 06/21/2024

Clinical Trial Details — Status: Completed

Administrative data
NCT number	NCT04455321
Other study ID #	KA19/170
Secondary ID
Status	Completed
Phase	N/A
First received
Last updated
Start date	March 15, 2020
Est. completion date	January 15, 2021

Study information
Verified date	February 2021
Source	Baskent University
Contact	n/a
Is FDA regulated	No
Health authority
Study type	Interventional

Clinical Trial Summary

This study aims to investigate the effect of suture materials with different absorption times on istmocel.

Recruitment information / eligibility
Status	Completed
Enrollment	102
Est. completion date	January 15, 2021
Est. primary completion date	August 1, 2020
Accepts healthy volunteers	No
Gender	Female
Age group	18 Years to 45 Years
Eligibility	Inclusion Criteria: - primary cesarean section - single pregnancy - 18-45 age Exclusion Criteria: - Diabetes mellitus disease - inflammatory bowel disease - systemic lupus erythematosus disease - rheumatoid arthritis disease - previous uterine surgery

Study Design

Related Conditions & MeSH terms

Intervention

Procedure:
• Suture materials effect on istmocel
Effect of suture materials with different absorption times on istmocel

Locations
Country	Name	City	State
Turkey	Baskent University Adana Dr. Turgut Noyan Hospital	Adana

Sponsors *(1)*
Lead Sponsor	Collaborator
Baskent University

Country where clinical trial is conducted

Turkey,

Outcome
Type	Measure	Description	Time frame	Safety issue
Primary	Istmocel	Istmocel area measurement with saline-infusion ultrasonography	Six months

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