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

Status

Completed

Phases

Study type

Interventional

Source

ClinicalTrials.gov

Registry ID

NCT04455321

Enrollment

102

Registered

2020-07-02

Start date

2020-03-15

Completion date

2021-01-15

Last updated

2021-02-09

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Istmocel, Suture, Complication

Keywords

rapid, suture material, istmocel

Brief summary

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

Interventions

PROCEDURESuture materials effect on istmocel

Effect of suture materials with different absorption times on istmocel

Study design

Allocation

RANDOMIZED

Intervention model

CROSSOVER

Primary purpose

PREVENTION

Masking

NONE

Intervention model description

Rapid vicryl will used in study group and vicryl will used in control group for uterine closure in cesarean section.

Eligibility

Sex/Gender

FEMALE

Age

18 Years to 45 Years

Healthy volunteers

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

Design outcomes

Primary

Measure	Time frame	Description
Istmocel	Six months	Istmocel area measurement with saline-infusion ultrasonography

Countries

Turkey (Türkiye)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026