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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register.
Register: ClinicalTrials.gov
Last refreshed on: 12 December 2020
Main ID:  NCT02338427
Date of registration: 12/01/2015
Prospective Registration: Yes
Primary sponsor: Centre Hospitalier Departemental Vendee
Public title: Capacity of Amylose Characterisation Compare by Immunohistochemistry and Proteomic Analysis IPA
Scientific title: Capacity of Amylose Characterisation Compare by Immunohistochemistry and Proteomic Analysis. Multicenter Prospective
Date of first enrolment: May 2016
Target sample size: 140
Recruitment status: Completed
URL:  https://clinicaltrials.gov/show/NCT02338427
Study type:  Interventional
Study design:  Allocation: N/A. Intervention model: Single Group Assignment. Primary purpose: Diagnostic. Masking: None (Open Label).  
Phase:  N/A
Countries of recruitment
France
Contacts
Name:     Hervé MAISONNEUVE, PH
Address: 
Telephone:
Email:
Affiliation:  Centre Hospitalier Départementel Vendée
Key inclusion & exclusion criteria

Inclusion Criteria:

- Upper age to 18 years

- Amylose diagnosis establish by tissue sample, after "Rouge Congo" coloration

- All patient with amylose identified by the two laboratory of anatomopathology

- Sample necessary for realized proteomic analysis

- No opposition at the participation of the study

- Patient sign an informed consent for biology collection

Exclusion Criteria:

- Tissue sample inadequate for apply immunohistochemistry or proteomic identification

- Patient trust, guardianship, under legal protection measure, deprived of freedom



Age minimum: 18 Years
Age maximum: N/A
Gender: All
Health Condition(s) or Problem(s) studied
Amyloidosis
Intervention(s)
Other: Proteomic analysis
Other: Immunohistochemistry
Primary Outcome(s)
Identification success of amylose by immunohistochemistry and proteomic analysis [Time Frame: Inclusion]
Secondary Outcome(s)
Secondary ID(s)
CHD 063-14
Source(s) of Monetary Support
Please refer to primary and secondary sponsors
Secondary Sponsor(s)
Ethics review
Results
Results available:
Date Posted:
Date Completed:
URL:
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