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Closure of Peritoneum at Cesarean Section and Postoperative Adhesion (cs adhesions)

B

Barzilai Medical Center

Status

Completed

Conditions

Cesarean Section
Adhesions

Treatments

Procedure: Closure of the peritoneum at cs

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

Objective: To determine the effect of non-closure of the visceral and parietal peritoneum during Cesarean section on the formation of adhesions.

Study design: A prospective randomized trial of 533 women undergoing primary Cesarean section; 256 were randomized to non closure and 277 to closure of the peritoneum. At a subsequent cesarean,he presence of adhesions and their severity was evaluated at several sites: between the layers of the abdominal wall, between the bladder and the abdominal wall, between bladder and uterus, between the uterus and the abdominal wall, and between the bowels and the pelvic organs. A cumulative adhesion score was calculated.

Enrollment

533 patients

Sex

Female

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Women undergoing primary CS

Exclusion criteria

  • Lack of consent by the patient or an urgent cesarean not allowing time to elicit an informed consent
  • Previous pelvic or abdominal surgery

Trial design

Primary purpose

Prevention

Allocation

Non-Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

533 participants in 2 patient groups

peritoneal closure
Active Comparator group
Treatment:
Procedure: Closure of the peritoneum at cs
Non closure of the peritoneum
No Intervention group

Trial contacts and locations

2

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Data sourced from clinicaltrials.gov

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