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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02855957
Other study ID # P120205
Secondary ID
Status Completed
Phase N/A
First received July 31, 2016
Last updated July 31, 2016
Start date June 2013
Est. completion date June 2016

Study information

Verified date July 2016
Source Assistance Publique - Hôpitaux de Paris
Contact n/a
Is FDA regulated No
Health authority France: Ministry of Health
Study type Interventional

Clinical Trial Summary

Our project aims to assess and validate an innovative prognostic and diagnostic test in order to i) define a severity index of the β-thalassemia according to the free α-Hb pool for a better management of the patient; ii) differentiate the α-thalassemia and β-thalassemia and iii) follow the evolution of this pool in response to treatment of patients. In the future, this prognostic test based on the measurement of free α-Hb pool may be suitable for routine laboratory practice. To carry out this project, cohort of 85 thalassemic patients and a group of 50 healthy volunteers have been recruited.


Recruitment information / eligibility

Status Completed
Enrollment 135
Est. completion date June 2016
Est. primary completion date July 2015
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria Patient

- Age = 18 years

- Written informed consent

- Affiliation to social security

- Known Hb Phenotypes

- Biological phenotype corresponding to a classical picture of thalassemia

Healthy volunteers

- Age = 18 years

- Written informed consent

- Affiliation to social security

Exclusion Criteria Patient

- Transfusion for less than 3 months

- Chronic active viral disease: hepatitis B, C, HIV

- Ongoing infections or known inflammatory diseases

- Hyper or Hypothyroidism known or subject treated by Levothyrox

- Active pathology or tumor remission for less than 5 years

- Oral corticosteroid

- Hemoglobinopathy other than thalassemia for patients

- Treatment by Hydroxyurea for more than 3 months

- Treatment by stimulating agent erythropoiesis for longer than 3 months

Healthy volunteers

- Transfusion for less than 3 months

- Chronic active viral disease: hepatitis B, C, HIV

- Ongoing infections or known inflammatory diseases

- Hyper or Hypothyroidism known or subject treated by Levothyrox

- Active pathology or tumor remission for less than 5 years

- Oral corticosteroid

- Genetically related to person with hemoglobinopathy

Study Design

Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Diagnostic


Related Conditions & MeSH terms


Intervention

Other:
Free a-Hb pool analysis


Locations

Country Name City State
France Henri Mondor Hospital Creteil

Sponsors (3)

Lead Sponsor Collaborator
Assistance Publique - Hôpitaux de Paris Institut National de la Santé Et de la Recherche Médicale, France, Paris 12 Val de Marne University

Country where clinical trial is conducted

France, 

References & Publications (1)

Vasseur C, Pissard S, Domingues-Hamdi E, Marden MC, Galactéros F, Baudin-Creuza V. Evaluation of the free a-hemoglobin pool in red blood cells: a new test providing a scale of ß-thalassemia severity. Am J Hematol. 2011 Feb;86(2):199-202. doi: 10.1002/ajh.21918. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Correlation between the pool of free a-Hb and genotype a and ß -globin of the patient and if necessary with the genotype AHSP gene Day 1 No
Secondary Correlation between the pool of free a-Hb and Hb value Day 1 No
Secondary Correlation between the pool of free a-Hb and Mean Corpuscular Hb Day 1 No
Secondary Correlation between the pool of free a-Hb and Mean Cell Volume Day 1 No
Secondary Correlation between the pool of free a-Hb and percent of reticulocytes Day 1 No
Secondary Correlation between the pool of free a-Hb and fetal Hb Day 1 No
Secondary Correlation between the pool of free a-Hb and erythrocyte enzymes Day 1 No