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

The University of Texas Health Science Center, Houston · NCT07182045

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Opens the official ClinicalTrials.gov record, with the study team’s contacts. Bored Studies doesn’t enroll anyone.

Key facts

Compensation
Not posted. Ask the study team before screening.
Who can join
Ages 18+ · Women only
Healthy volunteers
Accepted
Study type
Interventional · Not applicable
Target enrollment
120
US sites recruiting
1
Study start
September 18, 2025
Record last updated
May 14, 2026

Status re-checked against ClinicalTrials.gov within the last 12 hours.

What the study is about

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.

Being studied: Temporary clamping of uterine and ovarian vessels

Conditions: Myoma; Surgery

Eligibility criteria

Copied from the official record. The study team makes the final decision at screening.

Show full criteria

Inclusion Criteria

  • Patient undergoing minimally invasive myomectomy with either a single intramural or Submucosal fibroid =/>5cm or
  • Patients undergoing minimally invasive Myomectomy with =/> 5 fibroids

Exclusion Criteria

  • Pregnancy,
  • Age \<18yo,
  • Patients undergoing concomitant surgery such as endometriosis surgery,
  • Suspected malignancy

Recruiting US locations

  • Memorial Hermann Hospital

    Houston, TX 77030

    Site contact: Randa Jalloul, MD · 713-486-7700 · randa.j.jalloul@uth.tmc.edu

Study contacts (from the official record)

  • Randa Jalloul, MD · 3137128603 · randa.j.jalloul@uth.tmc.edu
All healthy volunteers studies in Texas →
Impact of Uterine and Ovarian Vessel Occlusion on Blood Loss in… (NCT07182045) | Bored Studies