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NCT06735625Recruiting

Pilot Study "AHSP as a Biomarker of Sickle Cell Disease in a Population of Adults and Children"

Source: ClinicalTrials.gov · Last updated 2 Apr 2025 · Not updated for over 12 months - ask the site whether it is still open

Brief summary (registry, in English)

Evaluation of AHSP concentration in total blood as a biomarker in adult and pediatric sickle cell patients

Status (registry)
Recruiting
Study type
Interventional
Enrollment
100 (estimated)
First submitted
11 Dec 2024
Start date
6 Mar 2025
Primary completion date
20 Mar 2026
Lead sponsor
Centre Hospitalier de Saint-Denis
NCT number
NCT06735625

What you commit to

  • Study type: Interventional
  • Planned participants: 100
  • From 6 Mar 2025 to the primary completion date, 20 Mar 2026
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Known hyper or hypothyroidism or subject treated with levothyroxine
  • Oral corticosteroid therapy in progress

Other illness

  • Hemoglobinopathies other than sickle cell disease (Criteria for Control Patients)
  • Chronic active viral disease: hepatitis B, C, HIV
  • Current infections or known inflammatory pathologies

Lab values

  • Hemoglobin disorder other than sickle cell disease (Criteria for Sickle Cell Patients)

Other

  • Transfusion less than 3 months ago
  • Active tumor pathology or remission for less than 5 years
  • Participation in interventional biomedical research
  • Opposition to participation in research by the patient if he is an adult, or by one of the two parents if the patient is a minor.
  • Non-affiliation to a social security system

Who the study is looking for

  • Adults: \> 15 years and 6 months
  • Pediatrics: ≥ 3 years and ≤ 15 years and 6 months
  • Known SS or Sβ0 phenotypes
  • 1 -Adults: \> 15 years and 6 months /Pediatrics: ≥ 3 years and ≤ 15 years and 6 months 2-Absence of Hemoglobinopathy 3-Follow-up for one of the following conditions (adults): Evaluation of hematological disease excluding hemoglobinopathy, evaluation of prolonged fever or inflammatory syndrome, initial or episodic evaluation of an auto-inflammatory disease or systemic disease, general health deterioration
  • -Follow-up for one of the following conditions (pediatrics): Suspected precocious puberty, growth delay, or neurodevelopmental disorder
  • 4-Blood sample planned as part of medical care

Age in the registry: 3 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Centre Hospitalier de Saint-Denis
Coordinator of this site? Confirm its status
Saint-DenisFranceRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.