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Clinical Trials/NCT04455321
NCT04455321CompletedNot Applicable

The Effect of Suture Materials With Different Absorption Times on Isthmocele: Prospective Randomized Study

Baskent University2 sites in 1 country102 target enrollmentStarted: March 15, 2020Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
102
Locations
2
Primary Endpoint
Istmocel

Study Overview

Brief Summary

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

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Crossover
Primary Purpose
Prevention
Masking
None

Eligibility Criteria

Ages
18 Years to 45 Years (Adult)
Sex
Female
Accepts Healthy Volunteers
No

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

Outcomes

Primary Outcomes

Istmocel

Time Frame: Six months

Istmocel area measurement with saline-infusion ultrasonography

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Selçuk Yetkinel

MD.

Baskent University

Study Sites (2)

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