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NCT Number: NCT07200778

Reducing Operative Blood Loss in Laparoscopic Myomectomy With Umbilico-uterine Trunk Clipping

the purpose of this study is to examine how Umbilico-uterine trunk occlusion reduces surgery-associated blood loss in Laparoscopic Myomectomy.

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Key information

Conditions

Laparoscopic Myomectomy

Age range

19 year–45 year

Sex eligibility

Female

Study type

Interventional

Phase

Not applicable

Primary location

Minia advanced laparoscopy unit

Minya, Egypt

Location status: Recruiting

Location contact

Mohamed abdelghfar, Lecturer

CONTACT

+20 10 61624335

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Age between 19 and 45
  • Symptoms of menorrhagia, pelvic pain, or infertility
  • Plan to have a laparoscopic myomectomy
  • Number of myomas ≤ 4, with the largest myoma measuring ≤ 9 cm

Exclusion criteria

  • Postmenopausal status
  • Dominant pedunculated subserosal FIGO classification (6-7)
  • Submucosal type of myoma FIGO classification (0-2)
  • Suspicion of malignant uterine or adnexal diseases
  • Major medical comorbidities or psychiatric illnesses that could affect follow-up and/or compliance
  • Refusal to participate or provide consent to the procedures.

Treatment and study plan

umbilico-uterine trunk occlusion

Procedure

participants will undergo umbilico-uterine trunk occlusion during laparoscopic myomectomy

local epinephrine infiltration

Procedure

participants will undergo local injections of epinephrine into the serosal and/or myometrium, covering the myoma before the uterine incision during laparoscopic myomectomy

Primary outcomes

  1. Operative Blood Loss

    Time frame: during operation

    The difference between the total amount of irrigation and suction will be used to compute operational blood loss

  2. Hemoglobin drop

    Time frame: 24 hours postoperative

    The difference between the preoperative and postoperative hemoglobin levels will be used to define the hemoglobin change.

Study contacts

Contact information is provided by the study sponsor or research team.

Mohamed abdelghfar, Lecturer

CONTACT

[email protected]

+20 10 61624335

Sponsors and collaborators

Lead sponsor

Minia University

Other

Registry information

Important dates

Study start
2025
Primary completion
2026
Study completion
2026
First posted
Oct 1, 2025
Registry last updated
Oct 7, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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