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Ultrasound Evaluation of Cesarean Scar After Uterotomy Closure With Barbed and Conventional Sutures

Ultrasound Evaluation of Cesarean Scar After Uterotomy Closure With Barbed and Conventional Sutures ; a Randomized Controlled Study

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03182010
Enrollment
110
Registered
2017-06-09
Start date
2017-08-31
Completion date
2020-08-31
Last updated
2017-06-14

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

Conditions

Cesarean Section Scar

Keywords

Cesarean section scar, Barbed suture, Conventional suture

Brief summary

The aim of this randomized control trial is to compare the residual myometrial thickness and the depth of cesarean section scar defect after uterine incision closure with barbed or conventional sutures.

Detailed description

The aim of this randomized control trial is to compare the residual myometrial thickness and the depth of cesarean section scar defect after uterine incision closure with barbed or conventional sutures. Primigravida patients undergoing transverse lower segment cesarean section will be included in the study.Cesarean section incision will be closed with double layers of continuous barbed or conventional sutures. Ultrasound examination will be performed 6 months after the operation to measure the residual myometrial thickness and the scar depth.

Interventions

DEVICECesarean section incision closure using barbed sutures

Cesarean section incision will be closed using a 24-cm × 24-cm 0 polydioxanone double-armed suture on a 26-mm half-circle reverse cutting needle( STRATAFIX™ Spiral PDO Knotless Tissue Control Device, Ethicon Inc , Somerville, NJ, USA ).Ultrasound examination will be performed 6 months after the operation to measure the residual myometrial thickness and the scar depth.

DEVICECesarean section incision closure using conventional sutures

Cesarean section incision will be closed using 1-0 polyglactin 910 suture(VICRYL™.; Ethicon Inc, Sommerville, NJ) .Ultrasound examination will be performed 6 months after the operation to measure the residual myometrial thickness and the scar depth.

Sponsors

Cairo University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
DIAGNOSTIC
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 50 Years
Healthy volunteers
No

Inclusion criteria

* Primigravida patients undergoing transverse lower segment cesarean section

Exclusion criteria

* Previous laparotomies * Postoperative fever * Patients with preterm pregnancies or in labor

Design outcomes

Primary

MeasureTime frameDescription
Residual myometrial thicknessSix months after cesarean sectionThickness of myometrium under the niche

Secondary

MeasureTime frame
Scar depthSix months after cesarean section

Countries

Egypt

Contacts

Primary ContactUsama M Fouda, Prof.
umfrfouda@yahoo.com01095401375

Outcome results

None listed

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