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NCT Number: NCT06882824

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

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.

Recruiting

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Key information

Age range

18 year–43 year

Sex eligibility

Female

Study type

Interventional

Phase

Not applicable

Primary location

CHU Clermont-Ferrand

Clermont-Ferrand, 63000, France

Location status: Recruiting

Location contact

Anne-Sophie GREMEAU

PRINCIPAL_INVESTIGATOR

Lise LACLAUTRE

CONTACT

[email protected]

+33473754963

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • 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
  • OTAU possible intraoperatively (Clip on uterine artery and tourniquet placement)
  • Speak and understand French
  • Affiliated with a social security scheme.

Exclusion criteria

  • 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
  • Patients with haemostasis disorders
  • Malnourished patients
  • Patients with hepatic or renal insufficiency
  • Pregnancy, suspected ectopic pregnancy and breast-feeding women.
  • Minors
  • Guardianship, curatorship, deprived of liberty, safeguard of justice

Treatment and study plan

myomectomy with placebo

Procedure

myomectomy after administration of placebo (control group)

myomectomy with misoprostol

Procedure

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

Primary outcomes

  1. 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.

    Time frame: during surgery

Secondary outcomes

  1. 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.

    Time frame: during surgery

  2. Compare Hemoglobin level (in g/L) between experimental and control groups

    Time frame: between day before surgery and day of surgery

  3. Compare Hemoglobin level (in g/L) between laparotomy and laparoscopy surgery

    Time frame: between day before surgery and day of surgery

  4. Compare between experimental and control groups: Patient age

    Time frame: at inclusion

  5. Compare between laparotomy and laparoscopy: Patient age

    Time frame: at inclusion

  6. Compare between experimental and control groups: Patient BMI

    Time frame: at inclusion

  7. Compare between laparotomy and laparoscopy: Patient BMI

    Time frame: at inclusion

  8. Compare between experimental and control groups: Patient medical history

    Time frame: at inclusion

  9. Compare between laparotomy and laparoscopy: Patient medical history

    Time frame: at inclusion

  10. Compare between experimental and control groups: Patient comorbidities

    Time frame: at inclusion

  11. Compare between laparotomy and laparoscopy: Patient comorbidities

    Time frame: at inclusion

  12. Compare between experimental and control groups: Size of myoma

    Time frame: at inclusion

  13. Compare between laparotomy and laparoscopy: Size of myoma

    Time frame: at inclusion

  14. Compare between experimental and control groups: FIGO classification of myoma

    Time frame: at inclusion

  15. Compare between laparotomy and laparoscopy: FIGO classification of myoma

    Time frame: at inclusion

  16. Compare between experimental and control groups: Number of myoma

    Time frame: at inclusion

  17. Compare between laparotomy and laparoscopy: Number of myoma

    Time frame: at inclusion

  18. Compare between experimental and control groups: Time between tablet intake and incision

    Time frame: day of surgery

  19. Compare between laparotomy and laparoscopy: Time between tablet intake and incision

    Time frame: day of surgery

  20. Compare between experimental and control groups: Total operative time

    Time frame: during surgery

  21. Compare between laparotomy and laparoscopy: Total operative time

    Time frame: during surgery

  22. Compare between experimental and control groups: Transfusion rate in number of RBCs (Red Blood Cells).

    Time frame: during surgery

  23. Compare between laparotomy and laparoscopy: Transfusion rate in number of RBCs (Red Blood Cells).

    Time frame: during surgery

  24. Compare between experimental and control groups: Immediate post-operative complications

    Time frame: up to 8 weeks after surgery

  25. Compare between laparotomy and laparoscopy: Immediate post-operative complications

    Time frame: up to 8 weeks after surgery

  26. Compare between experimental and control groups: Pain assessments at different times: VAS (Visual analogue scale from 0 : no pain to 10 : worst pain) at h+2, h+6 D1 M1

    Time frame: between 2 hours after surgery until 1 month post-operative

  27. Compare between laparotomy and laparoscopy: Pain assessments at different times: VAS (Visual analogue scale from 0 : no pain to 10 : worst pain) at h+2, h+6 D1 M1

    Time frame: between 2 hours after surgery until 1 month post-operative

  28. Compare between experimental and control groups: Length of hospital stay after surgery in days

    Time frame: up to one week after surgery

  29. Compare between laparotomy and laparoscopy: Length of hospital stay after surgery in days

    Time frame: up to one week after surgery

Study contacts

Contact information is provided by the study sponsor or research team.

Lise LACLAUTRE

CONTACT

[email protected]

+33473754963

Sponsors and collaborators

Lead sponsor

University Hospital, Clermont-Ferrand

Other

Registry information

Acronym: HEMOMYOC

Important dates

Study start
2025
Primary completion
2027
Study completion
2028
First posted
Mar 19, 2025
Registry last updated
Sep 24, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

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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