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Clinical Trials/NCT02282748
NCT02282748
Recruiting
Not Applicable

Swiss Longitudinal Cohort

Hypertension Excellence Centre Lucerne3 sites in 1 country1,000 target enrollmentOctober 2014

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Cardiovascular Risk Factors
Sponsor
Hypertension Excellence Centre Lucerne
Enrollment
1000
Locations
3
Primary Endpoint
Mortality
Status
Recruiting
Last Updated
6 years ago

Overview

Brief Summary

The planned research project is a prospective population-based cohort study, similar to the well-known Framingham study in the United States. So far, there is no similar research project in Switzerland.

It is planned to examine of three Swiss municipalities. Recruitment in a first Swiss municipality (Lostallo/Cama GR) started 2014 and ended in 2019. Overall, 496 participants were recruited in this municipality. The five-year follow-up in this municipality started in 2019. It is planned to start recruitment in a second Swiss municipality (Uznach SG) in 2020.

The examinations embrace a broad spectrum of measurements (for details the investigators refer to the published study protocol).

Registry
clinicaltrials.gov
Start Date
October 2014
End Date
September 2034
Last Updated
6 years ago
Study Type
Observational
Sex
All

Investigators

Sponsor
Hypertension Excellence Centre Lucerne
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Resident of Cama GR, Lostallo GR, or Uznach SG
  • Age ≥6 years (no upper age limit), for voluntary blood sample ≥18 years
  • Willing to participate in long-term study
  • Written informed consent (in participants ≥6 years and \<18 years signed by parents)

Exclusion Criteria

  • No exclusion criteria

Outcomes

Primary Outcomes

Mortality

Time Frame: 10 years

Secondary Outcomes

  • Heart function(10 years)
  • Cardiovascular events(10 years)
  • Autonomy(10 years)
  • Cognitive function(10 years)
  • Kidney function(10 years)
  • Nursing home admission(10 years)

Study Sites (3)

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