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Looks for markers in fluid and tissue of women with endometriosis

Studies biological markers in uterine fluid and tissue of women with endometriosis.

Plain-language title generated from the registry record
Registry title: Biomarkers in the Endometrial Fluid, Tissue, and Follicular Fluid of Moderate/Severe Endometriosis Patients

Key facts

Where
Stockholm, SwedenSee the site

Could this be for you?

Answer for yourself. This is not a decision: only the study team can say whether you can take part.

  • Are you between 18 and 40 years old?

Source: NCT07182643, who can take part

Where in Sweden

  • Karolinska Institute and Karolinska University Hospital HuddingeStockholm, SwedenNo longer taking part

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?
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Trial details

Who runs it
Region Stockholm
Trial code
NCT07182643
Record updated
19 September 2025
Original description
This study aims to explore biomarkers in the endometrial fluid and tissue of women with moderate to severe endometriosis, with a specific focus on those involved in pre-receptive endometrium and embryo implantation. This research has the potential to uncover diagnostic indicators of impaired pre-receptive endometrium, examine pathophysiological pathways, and identify future targets for therapeutic intervention. Ultimately, the findings may contribute to more personalized fertility treatments, offering new hope for women struggling with endometriosis-related infertility.Read full original descriptionShow less

An Exploratory Study of Biomarkers in the Endometrial Fluid, Tissue, and Follicular Fluid of Moderate/Severe Endometriosis Patients: a Prospective Study

This study aims to explore biomarkers in the endometrial fluid and tissue of women with moderate to severe endometriosis, with a specific focus on those involved in pre-receptive endometrium and embryo implantation. This research has the potential to uncover diagnostic indicators of impaired pre-receptive endometrium, examine pathophysiological pathways, and identify future targets for therapeutic intervention. Ultimately, the findings may contribute to more personalized fertility treatments, offering new hope for women struggling with endometriosis-related infertility.

Inclusion: Age 18-40 years old; Diagnosed with moderate/severe endometriosis by ultrasound or laparoscopy (patient group); Regular menstrual cycles 28-35 days; Speak English or Swedish and agree to participate in the study.

Exclusion: Major abdominal or pelvic surgery in the last 3 months; Pelvic inflammatory disease, endometritis, STD; Gynaecological cancers or other malignancies in the patient's history; A specific genetic disease that is diagnosed before PGT in women undergoing treatment; Pregnancy or lactation in the last 3 months; Uterine anomalies; Smoking (more than 10 cigarettes per day) or alcohol abuse; Immunosuppressing medicines.

ClinicalTrials.gov NCT07182643