Temporary Uterine Tourniquet Application Versus Local Myometrial Epinephrine Injection During Laparoscopic Myomectomy

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexFemale
Age18-45
SponsorMinia University

About this trial

While both local vasoconstrictors and tourniquet application are recognized methods for blood loss control, there is a paucity of head-to-head randomized controlled trials directly comparing these two distinct approaches in laparoscopic myomectomy. Existing data often compare these methods to no intervention or to other less common techniques. A direct comparison is essential to determine which method offers superior hemostasis with an acceptable safety profile in the laparoscopic setting. This study aims to address this gap in the literature.

Eligibility criteria

Qualifiers

Female patients aged 18-45 years.

Diagnosed with symptomatic uterine leiomyomas requiring laparoscopic myomectomy.

Presence of at least one myoma with a diameter ≥3 cm and ≤10 cm.

Patients with up to 3 myomas (to standardize surgical complexity).

Disqualifiers

Patients with more than 3 myomas or any myoma larger than 10 cm.

Patients with suspected uterine malignancy (e.g., leiomyosarcoma).

Patients with known bleeding disorders or on anticoagulant therapy that cannot be safely discontinued.

Patients with significant cardiovascular disease, uncontrolled hypertension, or arrhythmias (relative contraindications for epinephrine).

Trial design

Treatments tested in this trial

  • Temporary Uterine Tourniquet Application
  • Local Myometrial Epinephrine Injection

Treatment groups

37 Participants
are divided into 2 treatment groups

Locations

This trial has no locations

Sponsors and collaborators