RecruitingNot ApplicableNCT06882824

Prevention of HEMOrhagic Risk in Upper MYOmeCTomy by Use of Misoprostol.


Sponsor

University Hospital, Clermont-Ferrand

Enrollment

80 participants

Start Date

Mar 12, 2025

Study Type

INTERVENTIONAL

Conditions

Summary

In France, uterine fibroids or leiomyomas are the most common benign tumour in women of childbearing age. In 30% of cases, fibroids are symptomatic (menorrhagia, anaemia, pain), in which case surgical management is indicated. This is known as myomectomy, and can be performed by hysteroscopy, laparoscopy (laparoscopy) or laparotomy, depending on the number, size and position of the fibroids. Intraoperative bleeding is the main surgical difficulty. For this reason, a number of studies have focused on ways of minimizing the risk of bleeding. A good surgical indication, prevention of anaemia (iron deficiency) and transient occlusion of the uterine arteries during surgery help to reduce this risk. There are also drugs available to reduce intraoperative bleeding, but few studies have been carried out to assess their real effectiveness. One such product is Misoprostol, commonly used in gynecology. Its muscle-contracting properties suggest that it could have a beneficial effect on bleeding during surgery. What's more, this treatment has been used for many years and is reputed to be very well tolerated. The most frequent side effects are digestive, with a risk of abdominal pain in the form of cramps, nausea or vomiting. The investigators therefore decided to set up the HEMOMYOC study to demonstrate a significant reduction in bleeding during laparotomy or laparoscopic myomectomy after taking oral misoprostol in combination with transient occlusion of the uterine arteries, compared with placebo. It would seem that the ease of use and good tolerance of misoprostol, in combination with transient occlusion of the uterine arteries, could be of real benefit in preventing intraoperative morbidity in myomectomies, whatever the surgical approach. To date, no studies have been carried out in this area.


Eligibility

Sex: FEMALEMin Age: 18 YearsMax Age: 43 Years

Plain Language Summary

Simplified for easier understanding

This study is testing whether misoprostol — a medication that reduces bleeding — given before uterine fibroid removal surgery (myomectomy) can lower the risk of heavy bleeding during the procedure. **You may be eligible if...** - You are between 18 and 43 years old - You have uterine fibroids causing symptoms such as heavy bleeding, pain, or infertility - You are scheduled for laparoscopic or open fibroid removal surgery - You speak and understand French - You are covered by social security **You may NOT be eligible if...** - You have had prior major uterine surgery (other than hysteroscopic fibroid removal) - You are allergic to misoprostol or lactose - You take aspirin or blood thinners - You have bleeding disorders, liver or kidney disease, or are malnourished - You are pregnant, possibly pregnant, or breastfeeding Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

PROCEDUREmyomectomy with placebo

myomectomy after administration of placebo (control group)

PROCEDUREmyomectomy with misoprostol

myomectomiy after administration of misoprostol 400μg PO (experimental group)


Locations(1)

CHU Clermont-Ferrand

Clermont-Ferrand, Clermont-Ferrand, France

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NCT06882824


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