A prospective randomized controlled study of bilateral barb knot-free suture in the prevention of cicatrix defect in cesarean section incision

Status

Active, not recruiting

Phases

Phase 1

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR2400085961

Enrollment

Unknown

Registered

2024-06-21

Start date

2024-07-01

Completion date

Unknown

Last updated

2024-07-08

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

Conditions

cesarean scar defect

Interventions

experimental group:The uterus incision suture was made with bidirectional barb and knot-free suture

control group:The uterine incision was sutured with common Vichio thread

Eligibility

Sex/Gender

Female

Age

18 Years to 45 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: ? Normal menstrual cycle before pregnancy; ? First cesarean section; (3) Those who meet the indications for elective cesarean delivery (the main indications are macrosomia, breech pregnancy, transverse pregnancy, etc.); ? The pregnant women and their families understand the content of this study and voluntarily sign the informed consent.

Exclusion criteria

Exclusion criteria: Exclusion criteria: ? had a history of uterine surgery; ? There are complications or complications of pregnancy, such as gestational diabetes mellitus, gestational hypertension, placenta previa, complicated with malignant tumor, complicated with coagulation disorder, complicated with vaginitis, chorioamniotic infection and premature rupture of fetal membrane.

Design outcomes

Primary

Measure	Time frame
Width and depth of scar defect in cesarean section incision;	—

Secondary

Measure	Time frame
menstruation;	—

Countries

China

Contacts

Public ContactZhang Yu

Zhangzhou Affiliated Hospital of Fujian medical University

zhuangxueyi0505@126.com+86 150 6050 3190

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026