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NCT03892265Active, not recruiting

A Longitudinal Cohort Study to Evaluate Cardiovascular Risk Factors and Disease in Haiti

Source: ClinicalTrials.gov · Last updated 12 Feb 2026

Brief summary (registry, in English)

Investigators will establish a longitudinal cohort of \~3,000 adults \>18 years in Port-au-Prince using multistage random sampling, and follow them longitudinally to evaluate the prevalence and incidence of cardiovascular disease risk factors and diseases. Cardiovascular risk factors include hypertension, diabetes, obesity, dyslipidemia, kidney disease, poor diet, cigarette smoking, physical inactivity, and inflammation. Cardiovascular disease include angina and myocardial infarction, heart failure, stroke, and CVD mortality. It is anticipated that hypertension prevalence will be ≥10% in 18-30 year olds, that hypertension incidence will be \>10 events/1000 person years. Association of determinants and risk factors with CVD will also be examined. Whole blood, serum, plasma, stool, and urine samples will be biobanked for future studies.

Status (registry)
Active, not recruiting
Study type
Observational
Enrollment
3005 (actual)
First submitted
25 Mar 2019
Start date
8 Mar 2019
Primary completion date
1 Aug 2028
Lead sponsor
Weill Medical College of Cornell University
NCT number
NCT03892265

What you commit to

  • Study type: Observational
  • Participants enrolled: 3005
  • From 8 Mar 2019 to the primary completion date, 1 Aug 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 design.

Who cannot take part

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

Other illness

  • serious medical conditions or cognitive impairment preventing study participation as judged by research physicians,

Other

  • unable to speak and understand French or Creole.

Who the study is looking for

  • age \> or = 18 years, primary residence in the study area of Port-au-Prince (defined as having slept at the household at least once in the past two weeks and considers the household their primary residence with no plans to move in the next 24 months),
  • able to provide consent for study procedures,
  • agrees to study procedures, and
  • willing to be contacted at a new residence if a move occurs

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

Full criteria on ClinicalTrials.gov

Sites (1)

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

SiteCityCountrySite status
Les Centres GHESKIO
Coordinator of this site? Confirm its status
Port-au-PrinceHaitiUnknown status

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