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Uterine Closure in Caesarean SectionNCT06788899

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

An observational study of Uterine Closure in Caesarean Section, run by Assiut University.

Not yet recruiting

Opening soon. The study is approved but enrolment has not started yet. Sites may already take enquiries.

Sites and contacts
Official record
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Trial summary

Auditing of closure of uterine incision in Caesarean section in Assiut Women's Health Hospital. Read more about this study

Who is it for?
Any age, women only
Conditions the study is for
Uterine Closure in Caesarean Section
How many people
300 participants
Where
No sites listed yet
Study dates
Jan 2025to May 2026
Phase
Observational
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages Any age
  • Women only
  • Child, Adult, Older adult

Study population: All elective Caeserean sections with no medical or obestetric disorder

Who may be able to join

  • all elective Caesarean section

Who cannot join

  • Placenta previa
  • Chorioamionitis
  • PROM
  • Diabetic women
  • Immunocompromised women
  • Women with heart disease
Show all 10Show fewer
  • Women with renal or liver disease
  • Women on corticosteroids therapy
  • Preeclampsia
  • Women with hypertensive disorders

Trial locations and contacts

No sites are listed yet. Contact the study team or a site near you to ask about taking part.

Lobna Hassan AbdelRhman, Graduate contact

0201146398546

hassanlobna368@gmail.com

About this study

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

What is being measured

The primary outcome is the main question the study is designed to answer.

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

    Questionaire

    Measured: Through study completion an average of one year

Secondary outcomes (2)
  1. Decrease complications of caeserean section

    Questionaire

    Measured: Through study completion an average of one year

  2. Training of university staff

    Questionaire

    Measured: Through study completion an average of one year

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted23 Jan 2025
  2. Study startJan 2025 (estimated)
  3. Primary completionJan 2026 (estimated)
  4. Study completionMay 2026 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Other
Time perspective
Other
Enrolment
300 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06788899
Sponsor's protocol ID
Uterus closure
Status last verified
Dec 2024
First submitted
22 Dec 2024
Last updated
23 Jan 2025
Results posted
No
FDA-regulated drug
No
FDA-regulated device
No

Publications

  • Principles of Methodological Design of Clinical Audit. Arch Med Vol No:10 Iss No:2:2(1)

  • 1-Morrell C and Harvey G (1999) The Clinical Audit Handbook. Improving the quality of health care. London: Bailliere Tindall.(1)

  • Hauth JC, Owen J, Davis RO. Transverse uterine incision closure: one versus two layers. Am J Obstet Gynecol. 1992 Oct;167(4 Pt 1):1108-11. doi: 10.1016/s0002-9378(12)80048-2.

    PubMed 1415400

Questions about this trial

What is this clinical trial studying?

An observational study of Uterine Closure in Caesarean Section, run by Assiut University.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 1 inclusion and 10 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: opening soon, as of the sponsor's last update on 23 Jan 2025. Status can change between updates, so confirm with the study contact before making plans.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Contact Lobna Hassan AbdelRhman, Graduate (0201146398546, hassanlobna368@gmail.com), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

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). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT06788899, which also lists 3 linked publications.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 23 Jan 2025.

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