About this trial
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 criteria
This trial does not accept healthy volunteersQualifiers
Patient aged 18 to 43
Symptomatic myomas (bleeding, pain or infertility)
Indication for laparoscopic myomectomy Fibroma ≤ 10cm or number ≤ to 4 fibroids
Indication for myomectomy by laparotomy Fibroma > 10cm, Number > to 4 fibroids
Disqualifiers
History of major uterine surgery or myomectomy (excluding hysteroscopic myomectomy)
Allergy to misoprostol and lactose
Patients with hypersensitivity to misoprostol and/or other prostaglandins or to any of the product's excipients.
Patients taking aspirin or anti-coagulants
Trial design
Parallel
Treatments tested in this trial
myomectomy with placebo
Procedure/Surgerymyomectomy after administration of placebo (control group)
myomectomy with misoprostol
Procedure/Surgerymyomectomiy after administration of misoprostol 400μg PO (experimental group)
Treatment groups
Trial outcomes
Primary outcomes
Evaluation of intraoperative blood loss (in milliliters) during myomectomies with OTAU after administration of misoprostol 400μg PO (experimental group) versus placebo (control group) regardless of type of surgery.
Secondary outcomes
Evaluate intraoperative blood loss (in milliliters) during myomectomies with OTAU after administration of misoprostol 400μg PO (experimental group) versus placebo (control group) according to surgical technique, laparoscopy and laparotomy.
Compare Hemoglobin level (in g/L) between experimental and control groups
Compare Hemoglobin level (in g/L) between laparotomy and laparoscopy surgery
Compare between experimental and control groups: Patient age
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