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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02816580
Other study ID # PO14057
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date February 23, 2015
Est. completion date October 2, 2019

Study information

Verified date February 2022
Source CHU de Reims
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Epidemiological data from Europe have shown that around 30% of subjects aged over 65 years of age are pre-frail, and 15% are frail. Recent research has demonstrated that identifying frailty and implementing preventive measures can help to slow cognitive decline. Screening and treating frailty seem to be a good start towards preventing dependency. On the premise that this frailty is the result of more pronounced tissue alterations in certain elderly subjects, assessment of post-translational modification derived products (PTMDP) represents an innovative evaluation method. These include advanced glycation end-products (AGE), and carbamylation-derived products (homocitrulline). Indeed, the intensity of these modifications increases with ageing, and assessing the products resulting from these alterations could show the existence of differences according to frailty status. This would make it possible to adapt treatment accordingly in elderly subjects.


Recruitment information / eligibility

Status Completed
Enrollment 254
Est. completion date October 2, 2019
Est. primary completion date October 2, 2019
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 65 Years and older
Eligibility Inclusion Criteria: - With social security coverage - Accept to participate in the study and sign informed consent for the study and for the collection of biological samples Exclusion Criteria: - < 65 yo

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Blood collection


Locations

Country Name City State
France Chu de Reims Reims

Sponsors (1)

Lead Sponsor Collaborator
CHU de Reims

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary post-translational modification derived-products (PTMDP) quantification by Multidimensional Chromatography Coupled withTandem Mass Spectrometry (LC/LC-MS/MS) baseline
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