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UnknownNCT04358965

Tranexamic Acid Versus Vaginal Misoprostol in Abdominal Myomectomy

Evaluating Safety and Efficacy of Tranexamic Acid Versus Vaginal Misoprostol in Reducing Intraoperative Blood Loss During Abdominal Myomectomy

Status
Unknown
Phase
Phase 4
Study type
Interventional
Enrollment
162 (estimated)
Sponsor
Cairo University · Academic / Other
Sex
Female
Age
Healthy volunteers
Not accepted

Summary

the aim of the present study is to evaluate safety and efficacy of tranexamic acid versus vaginal misoprostol in reducing intraoperative blood loss during abdominal myomectomy

Conditions

Interventions

TypeNameDescription
DRUGintravenous tranexamic acidpatients will be given a single bolus IV injection of 15 mg/kg of tranexamic acid (TXA) 20 minutes before surgical incision plus one vaginal placebo tablet 60 minutes before skin incision.
DRUGvaginal misoprostolpatients will be given one vaginal misoprostol tablet (200 mcg) 60 minutes before skin incision and a normal saline IV bolus 20 minutes before surgical incision
DRUGplacebopatients will be given one vaginal placebo tablet 60 minutes before skin incision and a normal saline IV bolus 20 minutes before surgical incision

Timeline

Start date
2020-05-10
Primary completion
2020-10-10
Completion
2020-10-30
First posted
2020-04-24
Last updated
2020-04-24

Source: ClinicalTrials.gov record NCT04358965. Inclusion in this directory is not an endorsement.

Tranexamic Acid Versus Vaginal Misoprostol in Abdominal Myomectomy (NCT04358965) · Clinical Trials Directory