drugset / Trial / NCT05862428
Rectal Misoprostol in Women Undergoing Total Abdominal Hysterectomy for Intraoperative Blood Loss Reduction
RandomizedParallel-groupOpen-labelPrevention
Summary
Comparing of the intraoperative blood loss between group rectal misoprostol group and control group
Timeline
- Start
- 2022-02-18
- Primary completion
- 2022-09-26
- Completion
- 2022-09-26
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Misoprostol | Other / unclassified | 400 ug | Rectal |
Indications
No indication recorded.