Clinical Trials Directory

Trials / Unknown

UnknownNCT04357002

Intravenous Tranexamic Acid Versus Vaginal Dinoprostone in Abdominal Myomectomy

Evaluating Safety and Efficacy of Intravenous Tranexamic Acid Versus Vaginal Dinoprostone in Reducing Intraoperative Blood Loss During Abdominal Myomectomy: a Randomized Controlled Trial

Status
Unknown
Phase
Phase 4
Study type
Interventional
Enrollment
180 (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 intravenous tranexamic acid versus vaginal dinoprostone 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 dinoprostonepatients will be given one vaginal dinoprostone tablet (3mg) 60 minutes before skin incision and a normal saline IV bolus 20 minutes before surgical incision
DRUGvaginal placebopatients 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
2020-04-30
Primary completion
2020-10-01
Completion
2020-10-15
First posted
2020-04-22
Last updated
2020-04-22

Source: ClinicalTrials.gov record NCT04357002. Inclusion in this directory is not an endorsement.