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Clinical Trial Details — Status: Withdrawn

Administrative data

NCT number NCT03140735
Other study ID # PI2016_843_0035
Secondary ID
Status Withdrawn
Phase N/A
First received
Last updated
Start date July 3, 2017
Est. completion date June 20, 2023

Study information

Verified date July 2023
Source Centre Hospitalier Universitaire, Amiens
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Aortic valve pathology is the third most common cardiovascular disease after coronary artery disease and hypertension, which is responsible for severe morbidity and mortality in elderly patients and requires surgical treatment in its most severe form of progression. The purpose of this study is to find a link between arterial stiffness and degenerative aortic stenosis. If this link is established, arterial stiffness may become a medical therapeutic target in order to delay the evolution of the disease.


Recruitment information / eligibility

Status Withdrawn
Enrollment 0
Est. completion date June 20, 2023
Est. primary completion date June 20, 2023
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Patients over 18 years of age, without legal protection (guardianship or curatorship), - Stable hemodynamic status. - Affiliation to a social security scheme Exclusion Criteria: - Hemodynamically unstable patients: Systolic PA <10 cmHg, rapid peripheral pulse and spinning, mottling, obnubilation, oliguria, sweating, coma - History of significant valvulopathy other than an aortic stenosis, - Pregnancy. - Patient under tutelage or curatelle or deprived of public right.

Study Design


Intervention

Other:
Study the relationship between the arterial rigidity of large vessels and the presence and severity of degenerative aortic constriction
Study the relationship between the arterial rigidity of large vessels and the presence and severity of degenerative aortic constriction
Control group without heart disease
Control group without heart disease

Locations

Country Name City State
France CHU Amiens Picardie Amiens Picardie

Sponsors (1)

Lead Sponsor Collaborator
Centre Hospitalier Universitaire, Amiens

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Analysis of echocardiographic measurements of possible differences between average VOP and Sao i in terms of RA severities Analysis of echocardiographic measurements of possible differences between average VOP and Sao i in terms of RA severities 10 years
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