Clinical Trials Directory

Trials / Not Yet Recruiting

Not Yet RecruitingNCT07525687

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

Status
Not Yet Recruiting
Phase
N/A
Study type
Interventional
Enrollment
37 (estimated)
Sponsor
Minia University · Academic / Other
Sex
Female
Age
18 Years – 45 Years
Healthy volunteers
Not accepted

Summary

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.

Conditions

Interventions

TypeNameDescription
PROCEDURETemporary Uterine Tourniquet ApplicationThe tourniquet will be tightened just enough to achieve visible blanching of the uterus, indicating adequate vascular occlusion, but without excessive tension to avoid tissue damage
PROCEDURELocal Myometrial Epinephrine InjectionApproximately 5-10 mL of the diluted epinephrine will be injected into the myometrium surrounding each fibroid, specifically at the base of the myoma and along the planned incision line, using a laparoscopic injection needle.

Timeline

Start date
2026-04-20
Primary completion
2027-01-20
Completion
2027-01-20
First posted
2026-04-13
Last updated
2026-04-13

Source: ClinicalTrials.gov record NCT07525687. Inclusion in this directory is not an endorsement.