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NCT07263490Recruiting

PRIOR Study (Pre-eclampsia Risk In Oocyte Recipients)

PRIOR Study (Pre-eclampsia Risk In Oocyte Recipients) - Investigating Matching, Biomarkers and Outcomes.

Source: ClinicalTrials.gov · Last updated 13 Apr 2026

Brief summary (registry, in English)

The aim of this prospective observational cohort study is to investigate the pathophysiological mechanisms behind and risk of pre-eclampsia in women pregnant after fertility treatment with oocyte donation. The participants are included in of of two cohorts. One includes women pregnant after oocyte donation whereas the other includes women pregnant after IVF treatment with autologous oocytes. Participants will be followed throughout pregnancy with blood samples, blood pressure, clinical controls and ultrasound examinations. Clinical outcomes will be registered post-partum.

Status (registry)
Recruiting
Study type
Observational
Enrollment
462 (estimated)
First submitted
18 Nov 2025
Start date
21 Oct 2024
Primary completion date
31 Oct 2027
Lead sponsor
Copenhagen University Hospital, Hvidovre
NCT number
NCT07263490

What you commit to

  • Study type: Observational
  • Planned participants: 462
  • From 21 Oct 2024 to the primary completion date, 31 Oct 2027
  • 6 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

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 breast cancer
  • Present or previous chemotherapy/radiation therapy
  • Alcohol/drug abuse

Other illness

  • HIV/ hepatitis
  • Essential hypertension
  • Chronic kidney disease
  • Undiagnosed vaginal bleeding
  • Unregulated thyroid disease
  • Cardiovascular disease
  • Present or previous malignant disease

Age

  • Age \< 18 years

Other

  • BMI \> 35 kg/m2
  • Uterine malformations
  • Persisting ovarian cysts
  • Tumors in hypothalamus, pituitary, thyroid, or adrenal glands.
  • Known BRCA 1 or 2 gene
  • Breast feeding
  • Smoking

Who the study is looking for

  • Age \> 18 years
  • BMI \< 35 kg/m2
  • Normal wet smear within the past three years
  • Both nulli- and multiparous
  • Singletons and multiple gestations

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

Full criteria on ClinicalTrials.gov

Sites (6)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Copenhagen Fertility Center
Coordinator of this site? Confirm its status
CopenhagenDenmarkRecruiting
Trianglen Fertility Clinic
Coordinator of this site? Confirm its status
HellerupDenmarkRecruiting
Fertility Clinic, Herlev / Gentofte Hospital
Coordinator of this site? Confirm its status
HerlevDenmarkRecruiting
Fertility Clinic, Rigshospitalet
Coordinator of this site? Confirm its status
København ØDenmarkRecruiting
Sellmer Klinik
Coordinator of this site? Confirm its status
København SDenmarkRecruiting
Aleris Fertility
Coordinator of this site? Confirm its status
SøborgDenmarkRecruiting

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