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OpenTrials
Completed

NCT Number: NCT03095014

Myomectomy During Cesarean Section

Cesarean Myomectomy, safety and effect on uterine cavity.

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Key information

Conditions

Myomectomy

Age range

18 year–45 year

Sex eligibility

Female

Study type

Interventional

Phase

Phase 1

About this study

this study aims to compare between women who underwent Cesarean Myomectomy and those who underwent Cesarean section only regarding the procedure safety and whether uterine cavity was affected later on.

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

  • pregnant
  • full term
  • had uterine myoma

Exclusion criteria

  • history of coagulation disorder
  • antepartum hemorrhage
  • previous myomectomy
  • where additional operative procedures were performed

Treatment and study plan

Cesarean Myomectomy

Procedure

Myomectomy was done during Cesarean section

cesarean section

Procedure

Cesarean delivery

Primary outcomes

  1. Mean change in Haemoglobin in gm/dl

    Time frame: 24 hours

    pre-operative Haemoglobin minus post-operative Haemoglobin level

Secondary outcomes

  1. Duration of operation in hours

    Time frame: 2 hours

    time to complete the procedure

  2. intrauterine adesion adhesions

    Time frame: 3 months

    presence of uterine cavity adhesions

Sponsors and collaborators

Lead sponsor

Zagazig University

Other Gov

Registry information

Official study title

Cesarean Myomectomy : Safety and Risk of Intrauterine Synechiae

Important dates

Study start
2010
Primary completion
2015
Study completion
2016
First posted
Mar 29, 2017
Registry last updated
Mar 29, 2017

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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