Cesarean Section Clinical Trial
Official title:
Myomectomy During Cesarean Section: A Retrospective Cohort Study
| Verified date | August 2020 |
| Source | Mansoura University |
| Contact | n/a |
| Is FDA regulated | No |
| Health authority | |
| Study type | Observational |
To evaluate the value of myomectomy during delivery by cesarean section (CS) in pregnant women with uterine fibroids.
| Status | Completed |
| Enrollment | 178 |
| Est. completion date | December 31, 2019 |
| Est. primary completion date | December 31, 2019 |
| Accepts healthy volunteers | No |
| Gender | Female |
| Age group | 18 Years to 41 Years |
| Eligibility |
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. |
| Country | Name | City | State |
|---|---|---|---|
| n/a | |||
| Lead Sponsor | Collaborator |
|---|---|
| Mansoura University |
| Type | Measure | Description | Time frame | Safety issue |
|---|---|---|---|---|
| Primary | Deficit in hemoglobin level | Preoperative hemoglobin minus postoperative hemoglobin level (in gm/dl) | 24 hours | |
| Secondary | Operative time | Time to complete the procedure | 3 hours | |
| Secondary | Postoperative hospital stay period | Time from the end of operation to discharge from hospital | 7 days |
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