Vitamin D Status in Children With Sickle Cell Disease Living in Lyon, France

NCT ID: NCT04694976

Last Updated: 2023-07-20

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

130 participants

Study Classification

OBSERVATIONAL

Study Start Date

2021-02-04

Study Completion Date

2022-02-03

Brief Summary

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Vitamin D deficiency may be under-diagnosed in sickle cell disease French children. Therefore, the investigator need an epidemiologic study about the prevalence of vitamin D deficiency in this specific population. There are not specific guidelines neither testing nor treatment. The investigator propose to test vitamin D status in all children with sickle cell disease who are consulting their referring haematologist doctor or in the emergency ward.

Detailed Description

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Conditions

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Vitamin D Deficiency Sickle Cell Disease

Study Design

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Observational Model Type

OTHER

Study Time Perspective

PROSPECTIVE

Study Groups

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Sickle cell disease children from Lyon, France

Sickle cell disease children, followed in IHOPe (Institut d'Hématologie et d'Oncologie Pédiatrique) center, consulting their referring haematologist doctor or in emergency ward, with prescribed blood sample.

25-OH Vitamin D measure

Intervention Type BIOLOGICAL

As a complement to the off-study prescription, the investigator are taking two 1 mL tubes of extra blood to measure vitamin D, calcium, phosphorus, parathyroid hormone (PTH) and creatinine.

Interventions

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25-OH Vitamin D measure

As a complement to the off-study prescription, the investigator are taking two 1 mL tubes of extra blood to measure vitamin D, calcium, phosphorus, parathyroid hormone (PTH) and creatinine.

Intervention Type BIOLOGICAL

Eligibility Criteria

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Inclusion Criteria

* Children: under 18 years old
* Sickle cell any genetic type homozygous or composite heterozygous
* To receive an assessment independently of the study, during a presentation to the emergency ward and/or a follow-up consultation by the hematologist
* no parental opposition signed by at least one parent/legal representative and no child opposition
* social security beneficiary

Exclusion Criteria

* History of hematologic grafting
Maximum Eligible Age

17 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Hospices Civils de Lyon

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Valérie LAUNAY, MD

Role: PRINCIPAL_INVESTIGATOR

Urgences pédiatriques de l'Hôpital Femme Mère Enfant - Hospices Civils de Lyon

Locations

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Hôpital Femme Mère enfant - Urgences pédiatriques

Bron, , France

Site Status

Countries

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France

Other Identifiers

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ID-RCB

Identifier Type: OTHER

Identifier Source: secondary_id

69HCL20_0885

Identifier Type: -

Identifier Source: org_study_id

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