Other Clinical Trial - Epidemiologic Study of Persistent Polyclonal B-cell

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.

Interventional studies are often prospective and are specifically tailored to evaluate direct impacts of treatment or preventive measures on disease.

Observational studies are often retrospective and are used to assess potential causation in exposure-outcome relationships and therefore influence preventive methods.

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Clinical trials are conducted in a series of steps, called phases - each phase is designed to answer a separate research question.

Phase 1: Researchers test a new drug or treatment in a small group of people for the first time to evaluate its safety, determine a safe dosage range, and identify side effects.
Phase 2: The drug or treatment is given to a larger group of people to see if it is effective and to further evaluate its safety.
Phase 3: The drug or treatment is given to large groups of people to confirm its effectiveness, monitor side effects, compare it to commonly used treatments, and collect information that will allow the drug or treatment to be used safely.
Phase 4: Studies are done after the drug or treatment has been marketed to gather information on the drug's effect in various populations and any side effects associated with long-term use.

NCT number	NCT03296046
Study type	Observational
Source	Central Hospital, Nancy, France
Contact
Status	Completed
Phase	N/A
Start date	November 13, 2012
Completion date	December 31, 2015

Epidemiologic Study of Persistent Polyclonal B-cell Lymphocytosis (PPBL) — LPLB

Clinical Trial Summary

Clinical Trial Description

Study Design

Related Conditions & MeSH terms