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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT03263364
Other study ID # GIRODON PRTS 2015
Secondary ID
Status Recruiting
Phase N/A
First received August 23, 2017
Last updated August 25, 2017
Start date October 2016
Est. completion date October 2020

Study information

Verified date August 2017
Source Centre Hospitalier Universitaire Dijon
Contact François GIRODON
Phone 0380293031
Email francois.girodon@chu-dijon.fr
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Unexplained polycythemias are rare diseases, and therefore, the collection of data inherent to these diseases will not only improve their characterisation, but also allow stratification according to the risks and the course of the disease. The objective of this project is to constitute a database on the disease which will allow us to better understand it and in due course improve its management.

The GENRED project thus bears uniquely on the collection of information, which will be gathered throughout the usual management of patients for this type of disease.


Recruitment information / eligibility

Status Recruiting
Enrollment 150
Est. completion date October 2020
Est. primary completion date October 2020
Accepts healthy volunteers No
Gender All
Age group N/A and older
Eligibility Inclusion Criteria:

The characteristics of the patients included in the database will be described in terms of numbers and percentages for qualitative variables and in terms of means and standard deviations or medians and interquartile intervals for quantitative variables.

Exclusion Criteria:

The first step will be to exclude acquired secondary (pulmonary, renal and cardiac) or acquired primary (polycythemia vera due to JAK2 mutations) causes. The family history and the determination of serum EPO levels are very useful in the decision regarding which molecular tests should be performed first.

- patients without absolute erythrocytosis (i.e. without an increased red cell mass >125% of mean predicted value, or if the haematocrit is <60% in males or <56% in females.

- erythrocytosis related to polycythemia vera according to the 2008 WHO (World Health Organization) criteria

- Secondary erythrocytosis related to an obvious cause (renal lesions, chronic lung or heart diseases, endocrine lesions, miscellaneous tumours producing EPO, drugs such as androgens, hepatic lesions…)

- Low venous blood p50: the determination of p50 (percentage at which Hb is half saturated with oxygen) is very helpful is establishing the presence of a haemoglobin variant with high oxygen affinity or a rare 2,3-diphosphoglycerate (2,3-DPG) deficiency. In such a situation, a specific HBB, HBA1 and HBA2 mutation will be screened for using Sanger sequencing (these genes are not included in NGS analysis because of redundancy of pseudogenes).

In order to rule out non-informative erythrocytosis cases, a form including mandatory further tests must be filled in for a selection step. The required tests are: complete blood counts

- Blood electrolytes

- Arterial and venous gazes

- Serum erythropoietin dosage

- Liver function tests

- JAK2 mutations (both V617F and exon 12)

- Bone marrow aspirate and/or biopsy and/or endogenous BFU-E culture

- Abdominal ultrasound

- Lung function tests

Study Design


Related Conditions & MeSH terms

  • Hereditary Erythrocytosis/Idiopathic Erythrocytosis
  • Polycythemia

Locations

Country Name City State
France CHU Dijon Bourgogne Dijon
France CHU de NANTES Nantes

Sponsors (1)

Lead Sponsor Collaborator
Centre Hospitalier Universitaire Dijon

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Germline mutations that cause Hereditary Erythrocytosis/Idiopathic Erythrocytosis at baseline