Trials / Unknown
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
| Type | Name | Description |
|---|---|---|
| DRUG | intravenous tranexamic acid | patients 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. |
| DRUG | vaginal misoprostol | patients 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 |
| DRUG | placebo | patients 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.