NCT06049160View on ClinicalTrials.gov

Comparative Study Between Preoperative and Postoperative Rectal Misoprostol

NACompletedINTERVENTIONAL
Enrollment

128

Participants

Timeline

Start Date

August 31, 2023

Primary Completion Date

November 20, 2023

Study Completion Date

November 30, 2023

Conditions
Blood Loss, SurgicalBlood Loss, Postoperative
Interventions
DRUG

Misoprostol

All participants will be assigned for giving misoprostol rectally either preoperative or postoperative

Trial Locations (1)

Unknown

Faculty of medicine, Cairo University, Cairo

All Listed Sponsors
lead

Egymedicalpedia

INDUSTRY

NCT06049160 - Comparative Study Between Preoperative and Postoperative Rectal Misoprostol | Biotech Hunter | Biotech Hunter