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

ConditionLaparoscopic Myomectomy

Trial statusRecruiting

Trial phaseNot applicable

Trial typeInterventional

Biological sexFemale

Age19-45

SponsorMinia University

About this trial

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

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

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

Disqualifiers

Postmenopausal status

Dominant pedunculated subserosal FIGO classification (6-7)

Submucosal type of myoma FIGO classification (0-2)

Suspicion of malignant uterine or adnexal diseases

Trial design

Design model

Parallel

Treatments tested in this trial

umbilico-uterine trunk occlusion
Procedure/Surgery
participants will undergo umbilico-uterine trunk occlusion during laparoscopic myomectomy
local epinephrine infiltration
Procedure/Surgery
participants will undergo local injections of epinephrine into the serosal and/or myometrium, covering the myoma before the uterine incision during laparoscopic myomectomy

Treatment groups

66 Participants

are divided into 2 treatment groups

Group A: Group AExperimental treatment 1 intervention

Group B: Group BActive comparator 1 intervention

Trial outcomes

Primary outcomes

Operative Blood Loss

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

Time frame

during operation

Hemoglobin drop

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

Time frame

24 hours postoperative

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

Minia University

Lead sponsor

Source ClinicalTrials.gov

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