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Study identifier: NCT06882824 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

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

Condition: Myoma;Uterus · Myomectomy; Surgical Blood Loss  ·  Sponsor: University Hospital, Clermont-Ferrand

PhaseNA
Planned participants80
Who can joinFemale, 18 Years to 43 Years
Healthy volunteersNo

About this study

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 …

This description comes directly from the study's public registry record.

Talk to the study team

Lise LACLAUTRE  ·  +33473754963  ·  promo_internet_drci@chu-clermontferrand.fr

Always discuss trial participation with your own doctor first.

Locations (1)

CHU Clermont-FerrandClermont-Ferrand, Clermont-Ferrand, FranceRecruiting

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Source record: clinicaltrials.gov/study/NCT06882824