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NCT Number: NCT06788899

Clinical Audit on Uterine Closure During Caesarean Section in Assiut Women's Health Hospital

Auditing of closure of uterine incision in Caesarean section in Assiut Women's Health Hospital.

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Key information

Sex eligibility

Female

Study type

Observational

Who can participate

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

Inclusion criteria

  • all elective Caesarean section

Exclusion criteria

  • Placenta previa
  • Chorioamionitis
  • PROM
  • Diabetic women
  • Immunocompromised women
  • Women with heart disease
  • Women with renal or liver disease
  • Women on corticosteroids therapy
  • Preeclampsia
  • Women with hypertensive disorders

Treatment and study plan

Primary outcomes

  1. Improve performance of closure of Caesarean section. in Assiut Women health hospital according to NICE guidelines and National Library of Medicine

    Time frame: Through study completion an average of one year

    Questionaire

Secondary outcomes

  1. Decrease complications of caeserean section

    Time frame: Through study completion an average of one year

    Questionaire

  2. Training of university staff

    Time frame: Through study completion an average of one year

    Questionaire

Study contacts

Contact information is provided by the study sponsor or research team.

Lobna Hassan AbdelRhman, Graduate

CONTACT

[email protected]

0201146398546

Sponsors and collaborators

Lead sponsor

Assiut University

Other

Registry information

Important dates

Study start
2025
Primary completion
2026
Study completion
2026
First posted
Jan 23, 2025
Registry last updated
Jan 23, 2025

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.