Fibroids and Infertility - a Study of the Significance of Removal of Fibroids With Regard to Endometrial Receptivity

  • STATUS
    Recruiting
  • participants needed
    80
  • sponsor
    Oslo University Hospital
Updated on 19 February 2024
laparoscopy
infertility
leiomyoma
uterine myomectomy
gonadotropin-releasing hormone agonist
laparotomy
myomectomy
lh-rh analogs

Summary

We aim to explore some of the molecular factors that reduce fertility for women with leiomyomas, taking into account leiomyoma location, size, number and vascularity. Tissue samples from the endometrium and leiomyomas will be obtained during the mid secretory phase before and 3-6 months after surgical excision for a comprehensive search for key molecular derangements.

Description

Baseline medical information and standard questionnaire to record symptoms are collected from all participants and a gynaecological examination and a 2D and 3D vaginal ultrasonography including saline infusion sonography (SIS), if indicated, are performed. Blood samples for the biobank for extraction of germ line DNA and for identification of possible biomarkers are taken.

The women with submucosal leiomyomas will undergo hysteroscopic myomectomy and the women with intramural leiomyomas will undergo myomectomy per laparoscopy or laparotomy.

For the participants with intramural leiomyomas and the fertile/infertile controls, endometrial samples are taken with an endometrial suction curette in an outpatient setting at day 19-23 of the menstrual cycle. The endometrial sampling in the group of women with submucosal leiomyomas is being done during the hysteroscopic removal of the leiomyoma, also at day 19-23 of the menstrual cycle.

3-6 months after surgery, cycle day 19-23, endometrial samples will be taken from the women who have undergone myomectomy and ultrasound examination is being performed. The women with submucosal leiomyomas will undergo a second look hysteroscopy

Details
Condition UTERINE FIBROID
Age 18years - 40years
Treatment Transcervical resection of fibroids, Myomectomy per laparoscopy or laparotomy
Clinical Study IdentifierNCT04426760
SponsorOslo University Hospital
Last Modified on19 February 2024

Eligibility

Yes No Not Sure

Inclusion Criteria

Age: 18 to 40 years
Presence of leiomyoma(s)
Regular menstrual cycle (28 +/- 7 days)
Having had at least 2 normal menstrual cycles after ending the treatment if previously treated with GnRH analogue
Signed informed consent

Exclusion Criteria

No treatment indication (no symptoms and/or no desire for fertility)
Contraindication for surgery
Known endometriosis
Known PCOS
Untreated hydrosalpinx
Malignancy; gynaecological or other location
Pre-malignant or malignant pap smear or endometrial biopsy
Hormonal treatment including ulipristal acetat and levonorgestrel intrauterine device last three months before inclusion in the study
Ongoing treatment with GnRH analogue
Pregnancy last 3 months
Ongoing lactation
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