Clinical trial Recruiting at 1 site Observational Ages 18 and up Women only

Using hyperspectral imaging to assess endothelial dysfunction in preeclampsia

Official title: Systematic Evaluation of Endothelial Dysfunction as a Prognostic Marker for Outcomes in Women With Preeclampsia

Run by Heidelberg University · NCT06912477 · Data updated 2026-11-12

This study is testing if a special imaging technique can help doctors see how blood vessel function changes in pregnant women with preeclampsia to better understand the risks for both mom and baby.

Quick facts

Study typeObservational
Ages18 Years and up
SexWomen only
Enrollment385 (estimated)
SponsorHeidelberg University
Academic / other
Locations1 site (Heidelberg)
StatusRecruiting
StartedMay 8, 2025
Main results expectedDecember 2026
Study endsJuly 2027
Registry record updatedSeptember 4, 2026
Trial IDNCT06912477 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates for this study are women with singleton pregnancies who are 18 years or older and can provide informed consent.

Probably not a fit

Patients with severe fetal anomalies or those unable to provide consent, including those with language barriers or certain skin types, may not benefit from this study.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This observational study investigates the use of hyperspectral imaging as a diagnostic and prognostic tool for preeclampsia, a pregnancy-related hypertensive disorder. It aims to evaluate the changes in endothelial and vascular function associated with preeclampsia, which can lead to severe complications for both mother and fetus. The study will involve women with singleton pregnancies who are at least 18 years old and able to provide informed consent. By utilizing non-invasive hyperspectral imaging, the researchers hope to identify microcirculatory disturbances that may persist postpartum and contribute to long-term cardiovascular risks.

Why it matters

Potential benefit: If successful, this study could provide a new non-invasive method for early diagnosis and risk assessment of cardiovascular complications in women with a history of preeclampsia.

How similar studies have gone: While hyperspectral imaging has not been previously studied in the context of preeclampsia, its application in other medical fields has shown promise, suggesting potential for success in this novel approach.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* singleton pregnancies
* Age ≥ 18 years
* Patient's ability to provide consent
* written informed consent

Exclusion Criteria:

* Lack of consent
* Language barrier
* Dark to very dark skin type
* Severe fetal chromosomal/genetic/structural anomalies
* Laboratory changes in LDH, creatinine, or platelets due to other causes (e.g., isolated thrombocytopenia, e.g., immune thrombocytopenia, carcinoma)

Where it's running

  • Heidelberg University Hospital, Department of Gynecology and Obstetrics
    Heidelberg, Germany
    Recruiting

Study contacts

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.