Research of Predictive Factors to Immune Thrombopenic Purpura

NCT01648556 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 37

Last updated 2026-03-12

No results posted yet for this study

Summary

It is about a multicentric study prospective of more than patients' 60 years with a thrombopenia isolated of less than 100 G/L blood platelet without cause found to estimate so certain examinations realized in the diagnosis (medullary cytogenetics, dosage of the TPO, the Anti-platelet antibodies, isotopic lifetime of platelet) are in favour of the diagnosis of PTI.

Conditions

  • Purpura Thrombopenic

Interventions

OTHER

Blood tests and bone marrow biopsy repeated

Blood tests are realized for the dosage of the TPO, the dosage of the antiplatelet antibodies, to measure isotopic lifetime of platelet. The test in corticoids by the prednisone per os is realized too. The bone marrow biopsy is realized at the inclusion and during follow-ups if the haemogram is abnormal.

Sponsors & Collaborators

  • Assistance Publique Hopitaux De Marseille

    collaborator OTHER
  • Henri Mondor University Hospital

    collaborator OTHER
  • Hôpital Jean Verdier

    collaborator OTHER
  • CH Abbeville

    collaborator UNKNOWN
  • CH Compiègne

    collaborator UNKNOWN
  • CHRU BREST

    collaborator UNKNOWN
  • CHRU LILLE

    collaborator UNKNOWN
  • University Hospital, Angers

    collaborator OTHER_GOV
  • Centre Hospitalier Universitaire de Besancon

    collaborator OTHER
  • CHU CAEN

    collaborator UNKNOWN
  • CHU NICE

    collaborator UNKNOWN
  • CHU Rennes

    collaborator UNKNOWN
  • University Hospital, Toulouse

    collaborator OTHER
  • GROUPE HOSPITALIER INSTITUT CATHOLIQUE

    collaborator UNKNOWN
  • Centre Hospitalier Universitaire, Amiens

    lead OTHER

Principal Investigators

  • Jean Pierre MD MAROLLEAU, phD · CHU AMIENS

  • mathilde HUNAULT BERGER, Ph D · University Hospital, Angers

  • NADINE MAGY BERTRAND, PH D · Centre Hospitalier Universitaire de Besancon

  • Olivier FAIN, PH D · HOPITAL JEAN VERDIER, BONDY

  • BRIGITTE PAN PETESCH, D · CHU BREST

  • MICHEL LEPORRIER, PH D · University Hospital, Caen

  • BERTRAND GODEAU, PH D · CHU CRETEIL

  • PHILIPPE BIERLING, PH D · EFS IVRY SUR SEINE

  • LOUIS TERRIOU, PH D · CHRU LILLE

  • JEAN MARC DURAND, PH D · LA CONCEPTION MARSEILLE

Study Design

Allocation
NA
Purpose
DIAGNOSTIC
Model
SINGLE_GROUP

Eligibility

Min Age
60 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2013-01-15
Primary Completion
2022-12-28
Completion
2022-12-28

Countries

  • France

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01648556 on ClinicalTrials.gov