ClinicalTrials.Veeva

Menu

Swiss Longitudinal Cohort

H

Hypertension Excellence Centre Lucerne

Status

Enrolling

Conditions

Cardiovascular Risk Factors

Treatments

Other: No intervention

Study type

Observational

Funder types

Other

Identifiers

NCT02282748
SNCTP 000000612

Details and patient eligibility

About

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).

Enrollment

1,000 estimated patients

Sex

All

Ages

6+ years old

Volunteers

Accepts Healthy Volunteers

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

Trial contacts and locations

3

Loading...

Central trial contact

Andreas W Schoenenberger, MD; Paul Erne, MD

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems