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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05646888
Other study ID # RC31/22/0255
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date January 15, 2023
Est. completion date December 30, 2025

Study information

Verified date May 2023
Source University Hospital, Toulouse
Contact Pierre Cougoul, MD
Phone 531156265
Email cougoul.pierre@iuct-oncopole.fr
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Sickle cell disease (SCD) is an autosomal recessive genetic disorder linked to a single mutation on beta-globin chains. This leads to red blood cell deformation and chronic hemolysis which can result in vaso-occlusive events, anemia and vasculopathy. Pathophysiology is incompletely understood, and beyond red blood cell's abnormalities this involves hemostasis and innate immunity. The aim of our study is to describe the mechanisms of thrombo-inflammation during the vaso-occlusive crisis (VOC) in adults with sickle cell disease.


Description:

Pathophysiology of sickle cell disease is incompletely understood. The typical change of red blood cells into sickle cells lead to post-capillary stream abnormalities. This phenomenon is responsible of ischemia-reperfusion injuries. Chronic hemolysis is the second part of the pathophysiology. The consequences are vasoconstriction, endothelial lesions, chronic inflammation, hemostasis and platelets activation. Thrombo-inflammation concept was proposed by Tanguay to describe the interactions between hemostasis, platelets and innate immune cells (neutrophils polynuclear) during thrombotic process. Since this time, this concept was largely described in many clinical situations such as septicemia, COVID-19, coronaropathy, auto-immune diseases and sickle cell disease. In this project, we will study platelets activation and thrombo-inflammation markers in the beginning of a vaso-occlusive crisis, during the crisis and two months after the crisis. Blood samples will be collected during a routine care sample. Biological markers studied will be: - Soluble and surface markers of platelet activation; platelet-leukocytes aggregates - Plasmatic eicosanoids produced by platelets (TXB2) and immune cells - In vitro platelets reactivity; dynamic thrombus formation in normal and pathologic arterial blood stream - Platelet's inflammasome


Recruitment information / eligibility

Status Recruiting
Enrollment 10
Est. completion date December 30, 2025
Est. primary completion date November 30, 2025
Accepts healthy volunteers No
Gender All
Age group 18 Years to 99 Years
Eligibility Inclusion Criteria: - Patient with sickle cell disease diagnosis, hospitalized in emergency department and/or internal medicine department - Patient older than 18 years - Written consent to participate to the study - Patient with health insurance - Patient able to receive information about the study Exclusion Criteria: - Age < 18 years - Non consent to participate to the study - Women in pregnancy or breastfeeding - Treatment with aspirin or non steroidal anti inflammatory drug - Protected patient - Patient already involved in a study requiring collection of additional biological samples

Study Design


Intervention

Biological:
Blood sampling
the blood sample will be taken during a planned blood sampling

Locations

Country Name City State
France IUCT-Oncopole University Hospital Toulouse

Sponsors (1)

Lead Sponsor Collaborator
University Hospital, Toulouse

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary To evaluate mechanisms of platelet activation in the thrombo-inflammation process during a vaso-occlusive crisis. by flow cytometry analysis First 48h of hospitalization
Primary To evaluate mechanisms of platelet activation in the thrombo-inflammation process during a vaso-occlusive crisis. by flow cytometry analysis Day 13 (+/- 2 days)
Primary To evaluate mechanisms of platelet activation in the thrombo-inflammation process during a vaso-occlusive crisis. by flow cytometry analysis At day 60 (+/- 2 days)
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