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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT02807129
Other study ID # PO12140
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date January 2014
Est. completion date January 2024

Study information

Verified date October 2019
Source CHU de Reims
Contact Rachid MAHMOUDI
Phone 326784424
Email rmahmoudi@chu-reims.fr
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The aim of the study is to evaluate frailty in patients aged ≥ 65 years with cancer. The elderly population is very heterogeneous, it is necessary to evaluate these elderly patients before treatment to assess the risk-benefit balance. To date, this assessment relies on subjective clinical methods often not optimal, and slow to implement. An innovative method of evaluation could be the determination of elastin peptides. Indeed, the rate of these peptides, which are linked to serious conditions associated with age, rising inexorably with age and dose could help determine more objectively the type of treatment to offer older patients.

Expected results : This study will allow better identification of the group of frail elderly through more relevant biological marker that clinical assessment, often subjective and not available within a period compatible with the treatment of newly diagnosed cancer. This biological assessment will also enable optimal management of elderly patients in particular by allowing the geriatrician better efficiency.


Recruitment information / eligibility

Status Recruiting
Enrollment 300
Est. completion date January 2024
Est. primary completion date January 2024
Accepts healthy volunteers No
Gender All
Age group 65 Years and older
Eligibility Inclusion Criteria:

- 65 years or older

- diagnosis of cancer

- affiliation to a social security scheme

- Signed informed consent for the study and for the collection of biological samples

Exclusion Criteria:

- Patient protected by law (guardianship, trusteeship)

Study Design


Related Conditions & MeSH terms


Intervention

Biological:
blood withdrawn

urine collection


Locations

Country Name City State
France Chu Reims France 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 elastin peptides quantification up to 36 months
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