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Completed

NCT Number: NCT01723605

Insitu Repair Versus Uterine Exeriorization During Cesarean Section

Two types of uterine repair described during cesarean section, the investigators will try to compare between the two techniques.

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Key information

Conditions

Complications; Cesarean Section

Age range

18 year–42 year

Sex eligibility

Female

Study type

Interventional

Phase

Phase 3

Primary location

Faculty of medicine

Cairo, 12211, Egypt

About this study

Insitu repair of the uterus during cesarean section in Comparison to exteriorisation of the uterus during uterine closure

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • pregnant women

Exclusion criteria

  • liver disease
  • kidney disease
  • bleeding tendency
  • abnormal placentation
  • preeclampsia

Treatment and study plan

insitu repair

Procedure

closure of the uterine incision while the uterus initu

Other names: repair insitu

exteriorisation of the uterus

Procedure

uterine closure while the uterus is exteriorised

Other names: uterine closure with exteriorisation of the uterus

Primary outcomes

  1. Bowel movement

    Time frame: 12 hours

    Regain of bowel movement

Secondary outcomes

  1. Surgery duration

    Time frame: 2 hours

    The duration of intraoperative surgey

Sponsors and collaborators

Lead sponsor

Cairo University

Other

Registry information

Official study title

Insitu Repair Versus Uterine Exeriorization During Cesarean Section: A Randomised Controlled Trial

Important dates

Study start
2012
Primary completion
2013
Study completion
2013
First posted
Nov 8, 2012
Registry last updated
Dec 31, 2013

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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