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Tourniquet plus Tranexamic Acid versus Tourniquet plus Vaginal misoprostol during myomectomy

A Comparative Study Of Blood Loss Reduction During Open Myomectomy For Uterine Fibroids Using Tourniquet With Tranexamic Acid Versus Tourniquet With Vaginal Misoprostol: A Double-Blinded Randomized Trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
PACTR
Registry ID
PACTR202406615201194
Enrollment
78
Registered
2024-06-19
Start date
2024-06-24
Completion date
Unknown
Last updated
2026-09-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Uterine fibroids

Interventions

Tourniquet plus Intravenous Tranexamic Acid
Tourniquet plus vaginal misoprostol

Sponsors

Dr Ogwu Robinson
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: Inclusion Criteria I. Patients who had open abdominal myomectomy for uterine fibroids. II. Patients with pre-operative haemoglobin levels greater than or equal to 10g/dl III. Patients who gave written informed consent. IV. Patients who were willing to accept blood transfusion. V. Patients who were willing to accept Tranexamic Acid or Vaginal Misoprostol.

Exclusion criteria

Exclusion criteria: Exclusion Criteria I. Patients with known bleeding/ clothing disorder like thrombocytopenia with increased risk of bleeding. II. Patients with known allergic reaction to Tranexamic Acid or Misoprostol. III. Patients with any prior pelvic surgeries, such as previous myomectomy or Caesarean Section with increased risk of adhesions, prolonged surgery and bleeding. IV. Patients with co-existing endometriosis or adenomyosis from clinical history or findings from investigations. V. Patients with medical co-morbidity such as cardiac or renal disease

Design outcomes

Primary

MeasureTime frame
The blood loss at surgery

Secondary

MeasureTime frame
i. Need for blood transfusion in any of the participants in either arm of the study. ii. Any adverse drug reactions in any of the participants in either of the study arm.

Countries

Nigeria

Contacts

Public ContactRobinson Ogwu

Principal Investigator and Consultant Obstetrician and Gynaecologist

robinsonogwu80@gmail.com+2348023764840

Outcome results

None listed

Source: PACTR (via WHO ICTRP) · Data processed: Sep 19, 2026