BIOCEREVANCE: National Prospective Cohort for Monitoring Children With Severe Autoimmune Cytopenia.

Sponsor
University Hospital, Bordeaux (Other)
Overall Status
Completed
CT.gov ID
NCT04070612
Collaborator
(none)
122
62.2

Study Details

Study Description

Brief Summary

This study aims to study prospectively the clinical and paraclinical evolution and prognostic factors of autoimmune haemolytic anemias, Evans syndromes and chronic immunological thrombocytopenic purpura of children in France.

Condition or Disease Intervention/Treatment Phase
  • Other: Blood sample

Detailed Description

These autoimmune haematological diseases are rare diseases affecting the child, often very young, and serious and potentially life-threatening. International literature data are scarce, and include individual cases or small series.

They do not allow to determine an optimal therapeutic strategy in case of escape from the first-line treatments. Existing treatments (long-term corticosteroid therapy, immunoglobulins, splenectomy, immunosuppressants, chemotherapies, and more recently anti-CD20 antibodies) are inconsistently effective, and often associated with serious side effects.

The seriousness of these diseases, the therapeutic difficulties, and the absence of a targeted research project in France, led to the implementation of this study.

This study aims to study prospectively the clinical and paraclinical evolution and prognostic factors of autoimmune haemolytic anemias, Evans syndromes and chronic immunological thrombocytopenic purpura of children in France.

Study Design

Study Type:
Observational
Actual Enrollment :
122 participants
Official Title:
National Prospective Cohort for Monitoring Children With Severe Autoimmune Cytopenia
Actual Study Start Date :
Apr 4, 2007
Actual Primary Completion Date :
Jun 8, 2012
Actual Study Completion Date :
Jun 8, 2012

Arms and Interventions

Arm Intervention/Treatment
children with autoimmune haemolytic anemia

A blood sample of 2 times 2 to 5 ml additional maximum

Other: Blood sample
A blood sample of 2 times 2 to 5 ml additional maximum

Children with Evans syndrome

A blood sample of 2 times 2 to 5 ml additional maximum

Other: Blood sample
A blood sample of 2 times 2 to 5 ml additional maximum

Children with Immune thrombocytopenic purpura

A blood sample of 2 times 2 to 5 ml additional maximum

Other: Blood sample
A blood sample of 2 times 2 to 5 ml additional maximum

Outcome Measures

Primary Outcome Measures

  1. Complete sustainable remission (yes/no) for children with autoimmune haemolytic anemias [At the screening]

    Absence of clinical signs of anemia (grade 0) And Hemoglobin > 11 g / dl And reticulocytes <120,000 / mm3 And haptoglobin> 10 mg / dl And bilirubin <10 mg / l or 17 μmol / l And no specific treatment for at least 12 months

  2. complete remission (yes/no) for children with autoimmune haemolytic anemias [At the screening]

    Absence of clinical signs of anemia (grade 0) And Hemoglobin> 11 g / dl And reticulocytes <120,000 / mm3 Regardless of the level of haptoglobin or bilirubin And specific treatment in progress or interrupted for less than 12 months

  3. partial remission (yes/no) for children with autoimmune haemolytic anemias [At the screening]

    Clinical Signs of Anemia (Grade 1 or 2) Or Hemoglobin from 7 to 11 g / dl Or reticulocytes> 120,000 / mm3 Regardless of the level of haptoglobin or bilirubin

  4. no response (yes/no) for children with autoimmune haemolytic anemias [At the screening]

    Clinical Signs of Severe Anemia (Grade 3 or More) Or Hemoglobin <7 g / dl

  5. deceased patient (yes/no) for children with autoimmune haemolytic anemias [At the screening]

    Death yes/no

  6. Complete sustainable remission (yes/no) for children with chronic immunologic thrombocytopenic purpura [At the screening]

    Absence of clinical signs of haemorrhage (grade 0) And platelets> 100,000 / mm3 And no specific treatment for at least 12 months

  7. complete remission (yes/no) for children with chronic immunologic thrombocytopenic purpura [At the screening]

    Absence of clinical signs of haemorrhage (grade 0) And platelets> 100,000 / mm3 And specific treatment in progress or interrupted for less than 12 months

  8. partial remission (yes/no) for children with chronic immunologic thrombocytopenic purpura [At the screening]

    Clinical Signs of Hemorrhage (Grade 1 or 2) Or platelets between 30,000 and 100,000 / mm3

  9. no response (yes/no) for children with chronic immunologic thrombocytopenic purpura [At the screening]

    Clinical Signs of Severe Hemorrhage (Grade 3 or Greater) Or Platelets <30,000 / mm3

  10. deceased patient (yes/no) for children with chronic immunologic thrombocytopenic purpura [At the screening]

    Death yes/no

Eligibility Criteria

Criteria

Ages Eligible for Study:
N/A to 18 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Age strictly below 18 years of age at initial diagnosis

  • Affiliate child or beneficiary of a social security scheme

  • Child residing in metropolitan France

  • Diagnosis of autoimmune haemolytic anemias, Evans syndrome and / or chronic Immune thrombocytopenic purpura

  • Free, informed, written and signed consent

Exclusion Criteria:
  • Diagnosis of constitutional haemolytic anemia

  • Diagnosis of platelet constitutional disease

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

  • University Hospital, Bordeaux

Investigators

  • Principal Investigator: Yves PEREL, Pr, Bordeaux University Hsopital

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
University Hospital, Bordeaux
ClinicalTrials.gov Identifier:
NCT04070612
Other Study ID Numbers:
  • CHUBX 2005/18
First Posted:
Aug 28, 2019
Last Update Posted:
Aug 28, 2019
Last Verified:
Aug 1, 2019
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by University Hospital, Bordeaux
Additional relevant MeSH terms:

Study Results

No Results Posted as of Aug 28, 2019