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NCT05500989Recruiting

PlacEntal Acute Atherosis RefLecting Subclinical Atherosclerosis

Source: ClinicalTrials.gov · Last updated 5 Dec 2024 · Not updated for over 12 months - ask the site whether it is still open

Brief summary (registry, in English)

Pregnancy is considered a cardiovascular (CV) stress test, and complicated pregnancies are associated with an increased risk for cardiovascular disease (CVD) later in life. Moreover, it is known that often the pregnancy induced CV adaptation does not resolve completely after a short postpartum (PP) period and it is not clear whether these induced changes will resolve over a longer period of time (i.e. in the upcoming months/years after delivery). Understanding the cardiac adaptation during pregnancy and the reversal process in the postpartum period, as well as the factors that influence this these processes, may provide us not only insight in this mechanism, but may help us in identifying factors that may be target points for modification.

Status (registry)
Recruiting
Study type
Observational
Enrollment
226 (estimated)
First submitted
5 May 2022
Start date
1 Nov 2016
Primary completion date
31 Dec 2028
Lead sponsor
Maastricht University Medical Center
NCT number
NCT05500989

What you commit to

  • Study type: Observational
  • Planned participants: 226
  • From 1 Nov 2016 to the primary completion date, 31 Dec 2028
  • 1 site 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

  • Controls: Pre-existing chronic hypertension treated with antihypertensive medication or autoimmune disorder.

Other illness

  • Allergy or intolerance to glyceryl trinitrate, betablockers or iodinated contrast media.

Other

  • Women who do not want to be informed about the results of the tests, or women who do not want their general practitioner and specialist(s) to be informed about the test results

Who the study is looking for

  • Women aged ≥ 18 years
  • Controls: Women with an uncomplicated pregnancy at the moment of inclusion (i.e no foetal or maternal placental complications, such as pregnancy induced hypertension, preeclampsia or HELLP-syndrome, or small for gestational birth infancies)
  • Cases: Women diagnosed with a preeclamptic pregnancy at the moment of inclusion

Age in the registry: 18 years to - · Sex: Female · Accepts healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

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

SiteCityCountrySite status
Maastricht University Medical Center+ (MUMC+)
Coordinator of this site? Confirm its status
MaastrichtNetherlandsRecruiting

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