CHU Clermont-Ferrand
Clermont-Ferrand, 63000, France
Location status: Recruiting
NCT Number: NCT06882824
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.
Interested in participating?
Request Info18 year–43 year
Female
Interventional
Not applicable
Clermont-Ferrand, 63000, France
Location status: Recruiting
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
myomectomy after administration of placebo (control group)
myomectomiy after administration of misoprostol 400μg PO (experimental group)
Time frame: during surgery
Time frame: during surgery
Time frame: between day before surgery and day of surgery
Time frame: between day before surgery and day of surgery
Time frame: at inclusion
Time frame: at inclusion
Time frame: at inclusion
Time frame: at inclusion
Time frame: at inclusion
Time frame: at inclusion
Time frame: at inclusion
Time frame: at inclusion
Time frame: at inclusion
Time frame: at inclusion
Time frame: at inclusion
Time frame: at inclusion
Time frame: at inclusion
Time frame: at inclusion
Time frame: day of surgery
Time frame: day of surgery
Time frame: during surgery
Time frame: during surgery
Time frame: during surgery
Time frame: during surgery
Time frame: up to 8 weeks after surgery
Time frame: up to 8 weeks after surgery
Time frame: between 2 hours after surgery until 1 month post-operative
Time frame: between 2 hours after surgery until 1 month post-operative
Time frame: up to one week after surgery
Time frame: up to one week after surgery
Contact information is provided by the study sponsor or research team.
University Hospital, Clermont-Ferrand
Other
Acronym: HEMOMYOC
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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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