Actively Recruiting
Pilot Study "AHSP as a Biomarker of Sickle Cell Disease in a Population of Adults and Children"
Led by Centre Hospitalier de Saint-Denis · Updated on 2025-04-02
100
Participants Needed
1
Research Sites
97 weeks
Total Duration
On this page
Sponsors
C
Centre Hospitalier de Saint-Denis
Lead Sponsor
I
Inserm U955
Collaborating Sponsor
AI-Summary
What this Trial Is About
Evaluation of AHSP concentration in total blood as a biomarker in adult and pediatric sickle cell patients
CONDITIONS
Official Title
Pilot Study "AHSP as a Biomarker of Sickle Cell Disease in a Population of Adults and Children"
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Adults older than 15 years and 6 months
- Children aged 3 years to 15 years and 6 months
- Known SS or Sb20 sickle cell phenotypes
- Control adults older than 15 years and 6 months without hemoglobinopathy
- Control children aged 3 to 15 years and 6 months without hemoglobinopathy
- Control adults followed for hematological disease, prolonged fever, inflammatory syndrome, auto-inflammatory or systemic disease, or general health deterioration
- Control children followed for suspected precocious puberty, growth delay, or neurodevelopmental disorder
- Blood sample planned as part of medical care
You will not qualify if you...
- Hemoglobin disorders other than sickle cell disease (for sickle cell patients)
- Hemoglobinopathies other than sickle cell disease (for control patients)
- Blood transfusion within the last 3 months
- Chronic active viral diseases such as hepatitis B, C, or HIV
- Current infections or known inflammatory diseases
- Known hyperthyroidism or hypothyroidism or treatment with levothyroxine
- Active tumor disease or remission under 5 years
- Current oral corticosteroid therapy
- Participation in interventional biomedical research
- Opposition to participation by the patient or parents
- Not affiliated to a social security system
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Centre Hospitalier de Saint-Denis
Saint-Denis, France, 93200
Actively Recruiting
Research Team
S
Stéphanie NGO, Coordinating Investigator
CONTACT
S
Stéhanie COSSEC, Project Coordinator
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NON_RANDOMIZED
Model
PARALLEL
Primary Purpose
OTHER
Number of Arms
4
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