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Extra - Abdominal Versus Intra - Abdominal Repair of the Uterine Incision at Cesarean Section (EKAM)

S

Sheba Medical Center

Status

Completed

Conditions

Cesarean Wound Repair

Treatments

Procedure: Extra-abdominal repair
Procedure: Intra-abdominal repair

Study type

Interventional

Funder types

Other

Identifiers

NCT02373501
SHEBA-13-0494-EC-CTIL

Details and patient eligibility

About

To evaluate the effects of extra-abdominal repair of the uterine incision compared to intra-abdominal repair, and to study is there superiority of one technique over the other in terms of primary outcomes - operative( up to 4 hours after beginning of anesthesia) and post operative ( until day 4 after operation ) measurements , secondary outcomes, long-term outcomes and subjective outcomes.

PRIMARY OUTCOMES:

Intra - operative ( during the operation up to 4 hours from anesthesia )

  • nausea and vomiting
  • intraoperative hypotension
  • intraoperative pain

Post operative ( 4 hours from anesthesia and until release from hospital )

  • Blood transfusion
  • Venous thromboembolism
  • Febrile Morbidity
  • Endometritis
  • Wound Infection
  • Death

Subjective measures:

  • complain of pain 1-10 on day 1 post operative
  • time until walking
  • number of Days until having bowel movement
  • overall satisfactory

SECONDARY OUTCOMES:

  • Operative time
  • Estimated blood loss ( ebl ) - hemoglobin levels
  • Hospital stay

Full description

Cesarean section (CS) delivery is one of the most frequent surgical procedures to be performed worldwide and rates of CS delivery are increasing. In the late 80's, the rate of caesarean deliveries was 10-13 % in most of the big hospitals in Israel, and today it reaches up to 20-25% of all deliveries.

Numerous different surgical techniques for caesarean section delivery have been described, and the debate about the optimal caesarean technique to minimize surgical morbidity is ongoing.

One of the more controversial issues regarding caesarean technique is the manner by which uterine repair is conducted after delivery of the infant(s) and placenta.

Two techniques are being used depending on the uterus position during repairmen : In situ within the peritoneal cavity (intra- abdominal repair) or temporarily exteriorized onto the mother's abdomen (extra- abdominal repair).

Arguments in favor of temporary exteriorization include better visualization of any uterine extensions and more rapid uterine repair with consequent reductions in both operative time and intraoperative blood loss. Opponents of extraabdominal repair argue that this technique increases rates of intraoperative nausea and vomiting, adnexal trauma on replacement, possible infection, and venous air embolism (VAE) .

On this study the investigators prospectively recruit women who are about to be electively operated. The patients will be randomized into two groups - extra- abdominal versus intra-abdominal uterine repair using computer randomization. Different charts will be for first CS delivery versus recurrent CS delivery. The patient won't know to which group she was designated . On day three after operation - she will be asked to fill out questionnaire with one of the investigators for subjective measurements

Enrollment

95 patients

Sex

Female

Ages

18 to 42 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • singleton pregnancy
  • term pregnancy

Exclusion criteria

  • chorioamnionitis
  • uterine rupture
  • hysterotomy - adhesiolysis

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

95 participants in 2 patient groups

intra-abdominal repair
Experimental group
Description:
intra-abdominal repair of uterine incision, after delivery of the fetus and the placenta.
Treatment:
Procedure: Intra-abdominal repair
extra-abdominal repair
Experimental group
Description:
extra-abdominal repair of uterine incision, after delivery of the fetus and the placenta.
Treatment:
Procedure: Extra-abdominal repair

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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