Clinical Trials Directory

Trials / Unknown

UnknownNCT04080375

Preoperative Vaginal Dinoprostone Prior to Abdominal Myomectomy

the Effectiveness of Preoperative Vaginal Dinoprostone in Reducing Blood Loss During Abdominal Myomectomy:a Randomized Controlled Trial

Status
Unknown
Phase
Phase 3
Study type
Interventional
Enrollment
100 (estimated)
Sponsor
Cairo University · Academic / Other
Sex
Female
Age
18 Years – 50 Years
Healthy volunteers
Not accepted

Summary

The aim of the study is to compare the effectiveness of vaginal dinoprostone 3 mg versus placebo before myomectomy to decrease blood loss during and after the operation.

Conditions

Interventions

TypeNameDescription
DRUGDinoprostone 3 mgthe patient will take one vaginal tablet of 3 mg dinoprostone 1 hour before surgery
DRUGplacebothe patient will take one vaginal tablet of placebo 1 hour before surgery

Timeline

Start date
2019-09-10
Primary completion
2019-11-30
Completion
2019-12-10
First posted
2019-09-06
Last updated
2019-09-06

Source: ClinicalTrials.gov record NCT04080375. Inclusion in this directory is not an endorsement.

Preoperative Vaginal Dinoprostone Prior to Abdominal Myomectomy (NCT04080375) · Clinical Trials Directory