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NCT05780775Active, not recruiting

Lipid Balance in Adult Sickle Cell Patients

Study of Lipid Balance in Adult Sickle Cell SS or SC Patients at Steady State and According to Clinical Phenotypes and During Acute Complications Acronym : "HDL2"

Source: ClinicalTrials.gov · Last updated 10 Dec 2025

Brief summary (registry, in English)

This study aims to describe and/or searches for, in cohorts of adult sickle cell anemia (SCA) and SC sickle cell patients living in the French West Indies and followed by SCD Reference and Competence Centers: 1-lipids profiles and associations at steady state with occurrence of sickle cell disease (SCD) complications, 2-lipids profile evolution during and after prospective acute complications (vasoocclusive crises (VOC) and priapism), 3-lipids profile variation (inter /intra individuals) during 4 prospective years, 4- Genetic primary modulators of SCD complications, 5- insulin resistance (HOMA), free fatty acids and glycerol dosages, 6- lipids enzymes, lipidome and functionality of HDL in sub-groups of SCD population.

Status (registry)
Active, not recruiting
Study type
Interventional
Enrollment
116 (actual)
First submitted
12 Dec 2022
Start date
30 Nov 2022
Primary completion date
30 Nov 2027
Lead sponsor
Centre Hospitalier Universitaire de la Guadeloupe
NCT number
NCT05780775

What you commit to

  • Study type: Interventional
  • Participants enrolled: 116
  • From 30 Nov 2022 to the primary completion date, 30 Nov 2027
  • 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.

Other illness

  • Other hemoglobinopathies than sickle cell disease
  • Patient hospitalized for transfusion or bleeding in the last 3 months

Other

  • Pregnancy or lactation
  • Patient under judicial protection or without freedom
  • Patient not affiliated with a social security system

Who the study is looking for

  • Aged from 18 years and over
  • Be affected with Sickle cell anemia or SC sickle cell
  • Living in French Caribbean Islands of Guadeloupe or Martinique and followed by physicians issued from a French West Indies Sickle Cell Reference or Competence Center
  • At steady state in the last month (without acute complication)
  • To have given a written consent after information on the study.

Age in the registry: 18 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
Unité Transversale de la Drépanocytose
Coordinator of this site? Confirm its status
Pointe-à-PitreGuadeloupeUnknown status

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