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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT06357923
Other study ID # 23-PP-13
Secondary ID 2024-A00321-46
Status Not yet recruiting
Phase N/A
First received
Last updated
Start date May 1, 2024
Est. completion date May 1, 2026

Study information

Verified date April 2024
Source Centre Hospitalier Universitaire de Nice
Contact Andrea CICCONE
Phone 0492034702
Email ciccone.a@hu-nice.fr
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Recruitment on the RAV pole in consultation or day hospital. Competitive recruitment of subjects > 60 years of age respecting a male/female ratio = 1.


Description:

Recruitment on the RAV pole in consultation or day hospital. Competitive recruitment of subjects > 60 years of age respecting a male/female ratio = 1. After explanations and collection consent, collection of the patient's socio-demographic and medical characteristics and then carrying out a Peripheral venous blood sample (2 x 5ml tubes).


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 100
Est. completion date May 1, 2026
Est. primary completion date May 2, 2024
Accepts healthy volunteers No
Gender All
Age group 60 Years to 99 Years
Eligibility Inclusion Criteria: - Men and women over 60 years of age. Exclusion Criteria: - Inability to Understand Consent, - Non-Security Beneficiaries - social, subjects protected by law, subjects deprived of liberty, - history of breast cancer, - brain tumor, - melanoma, - colon cancer, - lung cancer, - prostate cancer, - lymphoma, - myeloma, - syndrome myelodysplastic/myeloproliferative, - leukemia, - history of radiation therapy.

Study Design


Related Conditions & MeSH terms


Intervention

Diagnostic Test:
dosage
Presence of mutation on the gene panel and Frequency of allele variation

Locations

Country Name City State
France Chu de Nice Nice

Sponsors (1)

Lead Sponsor Collaborator
Centre Hospitalier Universitaire de Nice

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Expression level of LAMP2 (protein and isoform A and B mRNA) dosage day 0
Secondary Presence of mutation in the "Oncomin Myeloid Reasearch Assay" gene panel targeting approximately 40 Different genes dosage day 0
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