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Myomectomy During CS: A Retrospective Cohort Study

Myomectomy During Cesarean Section: A Retrospective Cohort Study

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03270605
Enrollment
178
Registered
2017-09-01
Start date
2015-01-01
Completion date
2019-12-31
Last updated
2020-09-01

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cesarean Section, Uterine Fibroid

Brief summary

To evaluate the value of myomectomy during delivery by cesarean section (CS) in pregnant women with uterine fibroids.

Interventions

PROCEDUREMyomectomy

Surgical removal of uterine fibroid

Sponsors

Mansoura University
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 41 Years
Healthy volunteers
No

Inclusion criteria

* Women who underwent elective CS with presence of uterine fibroid during the index pregnancy documented antenatal and at surgery

Exclusion criteria

* Antepartum hemorrhage * Blood diseases or bleeding tendencies. * Medical conditions complicating pregnancy. * Performed another surgical procedure at CS other than myomectomy.

Design outcomes

Primary

MeasureTime frameDescription
Deficit in hemoglobin level24 hoursPreoperative hemoglobin minus postoperative hemoglobin level (in gm/dl)

Secondary

MeasureTime frameDescription
Operative time3 hoursTime to complete the procedure
Postoperative hospital stay period7 daysTime from the end of operation to discharge from hospital

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026