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Heart Rate, Baroreflex Sensitivity and Cardiovascular Morbidity and Mortality in the Population

Heart Rate, Baroreflex Sensitivity and Cardiovascular Morbidity and Mortality in the Population. The Paris Prospective Study III

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT00741728
Acronym
PPSIII
Enrollment
10157
Registered
2008-08-26
Start date
2008-05-13
Completion date
2032-12-01
Last updated
2026-02-11

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Blood Pressure, Cardiovascular Disease, Community Based Study, Sudden Death

Keywords

epidemiology, risk factors, heart rate, baroreflex sensitivity, sudden death

Brief summary

The aim of the present Paris Prospective Study III (PPS3) is (1) to assess the determinants of the regulation of heart rate and blood pressure variations and carotid properties (under different physiologic stimulations) and (2) to evaluate the respective contribution of heart rate, blood pressure variations and carotid properties to cardiovascular morbidity and mortality including sudden death during 10 years at least in healthy considered subjects.

Detailed description

Overall, 10 157 men and women have been recruited during May 2008 and June 2012 for an extensive clinical examination including a 2h holter electrocardiography (ECG), a carotid doppler echo tracking, a step test, as well as blood and DNA collections. Since then, the cardiovascular morbidity and mortality of the participants is being followed up for 10 years at least and will continue up to 2032.

Interventions

OTHERSpider flash ECG, high-precision carotid echo-tracking, step test

cardiac rhythm recorded during health check up, vascular aging parameters and baroreflex sensitivity recorded during carotid echotracking of the right common carotid artery , step test during 2 minutes

Sponsors

Institut National de la Santé Et de la Recherche Médicale, France
Lead SponsorOTHER_GOV

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
50 Years to 75 Years
Healthy volunteers
Yes

Inclusion criteria

* 50-75 years, French speaking, given consent for genetic analysis, * written consent for participating in the study

Exclusion criteria

* \<50 years and \>75 years, * no French speaking, * current pregnancy, * chronic severe disease, * disagreement for genetic analysis, * step test considered as non possible or non advisable by medical decision.

Design outcomes

Primary

MeasureTime frameDescription
cardiovascular disease (CVD)through study completion, an average of 24 yearsincident coronary heart disease (CHD), stroke, sudden death, mortality

Secondary

MeasureTime frameDescription
heart rate parameters and baroreflex sensitivity4 Yearsas measured on the Spider Flash ECG and the carotid echotracking
other CVD outcomesthrough study completion, an average of 24 yearsheart failure, arterial aneurysms, venous thromboembolism (VTE), pulmonary embolism, arrhythmic events (atrial fibrillation, flutter)

Countries

France

Contacts

STUDY_DIRECTORXavier Jouven, MD, PhD

INSERM and APHP

PRINCIPAL_INVESTIGATORJean-Philippe Empana, MD, PhD

Institut National de la Santé Et de la Recherche Médicale, France

PRINCIPAL_INVESTIGATORPierre Boutouyrie, MD, PhD

INSERM and APHP

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 1, 2026