Suspended

VICTORMesure de l'Index de Pression Systolique de Cheville après Test d'Effort Maximal.

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What is being tested

Exercise test

Other
Who is being recruted

Cardiovascular Diseases

Over 18 Years
+2 Eligibility Criteria
See all eligibility criteria
How is the trial designed

Diagnostic Study

Interventional
Study Start: September 2009
See protocol details

Summary

Principal SponsorUniversity Hospital, Angers
Last updated: August 2, 2022
Sourced from a government-validated database.Claim as a partner

Study start date: September 17, 2009

Actual date on which the first participant was enrolled.

Estimate the response of ankle to brachial pressure index to incremental maximum exercise in subjects free from prior cardiovascular disease. Estimate morbi-mortality of included patients over a 5 years follow up.

Principal SponsorUniversity Hospital, Angers
Last updated: August 2, 2022
Sourced from a government-validated database.Claim as a partner

Protocol

This section provides details of the study plan, including how the study is designed and what the study is measuring.
Design Details

1760 patients to be enrolled

Total number of participants that the clinical trial aims to recruit.

Diagnostic Study

Diagnostic studies focus on improving how we detect or confirm a disease. They test new tools or techniques that could provide faster or more accurate diagnoses.



Eligibility

Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.
Conditions
Criteria

Any sex

Biological sex of participants that are eligible to enroll.

Over 18 Years

Range of ages for which participants are eligible to join.

Healthy volunteers allowed

If individuals who are healthy and do not have the condition being studied can participate.

Conditions

Pathology

Cardiovascular Diseases

Criteria

1 inclusion criteria required to participate
18 years old and more

1 exclusion criteria prevent from participating
patient with recent cardiovascular event

Study Plan

Find out more about all the medication administered in this study, their detailed description and what they involve.
Treatment Groups
Study Objectives

One single intervention group is designated in this study

This study does not include a placebo group 

Treatment Groups

Group I

Ankle pressure Index measure before and after Maximal Exercise Tests

Study Objectives

Primary Objectives

Secondary Objectives

Study Centers

These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.

This study has 1 location

UHAngers

Angers, FranceOpen UHAngers in Google Maps
SuspendedOne Study Center