Impact of Uterine and Ovarian Vessel Occlusion on Blood Loss in High Burden Minimally Invasive Myomectomy.

Part of paid clinical trials in Houston, Texas.

Sponsor
The University of Texas Health Science Center, Houston
Study ID
NCT07182045
Status
Recruiting
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Conditions

  • Myoma
  • Surgery

Eligibility Criteria

Sex
FEMALE
Age
18 Years - N/A
Healthy Volunteers
Accepted

Interventions

  • Temporary clamping of uterine and ovarian vessels — OTHER
    Surgeon will temporarily clamp uterine and ovarian vessels.

Study Details

This study hypothesizes that temporary bilateral uterine and utero-ovarian artery occlusion with laparoscopic clamps at time of minimally invasive myomectomy will lead to a decreased blood loss at time of myomectomy compared to minimally invasive myomectomy without temporary occlusion.

Key Dates

Start date
Sep 18, 2025
Status verified
May 2026
Primary completion
Sep 30, 2028
Completion
Sep 30, 2029

Study Design

Enrollment
120 participants (estimated)
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT

Arms

  • Experimental: Temporary vessel clamps
    Use of temporary laparoscopic vessel clamps on uterine and ovarian vessels
  • No Intervention: No Temporary vessel clamps
    No use of vessel clamps

Primary Outcome Measure

Estimated blood loss [ Time Frame: Intraoperative (during surgery, which is < 24 hours) ]

Central Contacts

Locations (1)

FacilityCityStateZIPSite coordinators
Memorial Hermann HospitalHoustonTexas77030
Randa Jalloul, MD
[email protected]
713-486-7700

Find similar trials in Houston, TX

By research site
Memorial Hermann Hospital· Houston, TX

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