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NCT05637073Withdrawn

Effect of Management of the Endometrioma on Ovarian Reserve

Impact of the Type of Treatment of the Endometrioma on Ovarian Reserve

Source: ClinicalTrials.gov · Last updated 8 Jul 2026

Reason given: After months of attempts, an insurmountable difficulty has arisen in recruiting patients at the main center, in addition to the retirement of the principal investigator.

Brief summary (registry, in English)

Investigators aimed at comparing the impact on ovarian reserve of three usual-care management options of endometrioma, laparoscopic cystectomy (LC), hormonal treatment with daily dienogest (HT), or mere ultrasound control (UC). Ovarian reserve will be measured by the effect on the circulating levels of anti-Mullerian hormone (AMH). Secondary objectives will be effect on pelvic pain, other symptoms, sexual function, quality of life, progression in size of the endometrioma, impact on work productivity and activity impairment, and satisfaction with treatment. Participants will be followed by up to one year.

Status (registry)
Withdrawn
Study type
Observational
Enrollment
0 (actual)
First submitted
22 Oct 2022
Start date
14 Mar 2023
Primary completion date
2 Jun 2026
Lead sponsor
University of Valencia
NCT number
NCT05637073

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Previous ovarian surgery;
  • Previous pathologies involving the ovary, including other ovarian tumors, polycystic ovaries, or pelvic inflammatory disease;
  • Previous diagnosis of cancer treated with chemotherapy or local radiotherapy;
  • Unhealthy habits, including smoking, alcohol consumption above social level, or illicit drugs;
  • Current or previous use of hormonal contraceptives, Gonadotropin-Releasing Hormone (GnRH) analogues, any drug with a known effect on endometriosis, or any drug under investigation, for what a washing up period of 6 months will be required in all cases.

Other illness

  • Diseases affecting the endocrine system, diabetes, thyroid, hyperprolactinemia, or the immune system (lupus, Crohn,…);

Other

  • Genesic wish;
  • Endometrioma >7 cm;
  • Insufficient level of autonomy for unrestrictedly signing informed consent;

Who the study is looking for

  • Caucasian premenopausal women between 18-39 years with the diagnosis of endometrioma, one or more, with a diameter of up to 7 cm by endovaginal ultrasound. Body mass index comprised between 17-30 Kg/m2

Age in the registry: 18 years to 39 years · Sex: Female · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (2)

Sites in registry order. Save your city in your profile to sort them by distance.

SiteCityCountrySite status
Hosp Clinico Universitario-INCLIVAValenciaSpainUnknown status
University Hospital PoznanPoznanPolandUnknown status

Are you the coordinator? Confirm the details

This page is information, not medical advice. Discuss any trial with your doctor.