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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03296046
Other study ID # 2011/PSS/LPLB/LESESVE//MS
Secondary ID
Status Completed
Phase N/A
First received September 22, 2017
Last updated September 27, 2017
Start date November 13, 2012
Est. completion date December 31, 2015

Study information

Verified date September 2017
Source Central Hospital, Nancy, France
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The main purpose of this study is the description of all French cases of PPBL and the establishment of minimal criteria for the pathology diagnosis and its follow-up.

The secondary objective is the immunologic and genetic characterization of lymphoid cells causing the disease.


Recruitment information / eligibility

Status Completed
Enrollment 100
Est. completion date December 31, 2015
Est. primary completion date December 31, 2015
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- PPBL diagnosis established during a previous medical visit

Exclusion Criteria:

Study Design


Related Conditions & MeSH terms


Intervention

Biological:
Blood test
30 ml

Locations

Country Name City State
France group GFHC and intergroup LLC (GCFLL-MW / GOELAMS) Marseille
France CHRU de Nancy - Hopitaux de Brabois VandÅ“uvre-lès-Nancy

Sponsors (1)

Lead Sponsor Collaborator
Central Hospital, Nancy, France

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Relevant medical history Baseline
Primary Complete blood count Baseline
Primary Administration of first-line treatment or not Baseline
Secondary Lymphocyte phenotype Baseline