Central Nervous System Vascular Changes in Adult Sickle Cell Disease and the Effect of Treatment With Simvastatin
Primary Purpose
Sickle Cell Disease, Stroke
Status
Unknown status
Phase
Phase 1
Locations
Brazil
Study Type
Interventional
Intervention
Simvastatin 40mg
Sponsored by
About this trial
This is an interventional prevention trial for Sickle Cell Disease
Eligibility Criteria
Inclusion Criteria:
- Diagnosis of Sickle Cell Disease
Exclusion Criteria:
- Previous stroke
- Some relevant concomitant clinical condition (cancer, AIDS, inflammatory / autoimmune diseases, etc.).
- Pregnancy
- Individuals considered to be vulnerable (minors,institutionalized individuals, patients with a history of psychiatric illness with cognitive impairment or incapacity)
Sites / Locations
- Hematology and Transfusion Medicine Center
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
Treatment
Arm Description
Treatment: Simvastatin 40mg/day
Outcomes
Primary Outcome Measures
Stroke prevention
Number of patients in the cohort presenting srtoke or silent infarction detected at MRI
Secondary Outcome Measures
Improvement of hemodynamic parameters in MRI:velocity
Evaluation of changes in vessel segment-averaged velocity (cm/s) in the Circle of Willis
Improvement of hemodynamic parameters in MRI: lumen area
Evaluation of changes in vessel lumen area (mm2) in the Circle of Willis
Improvement of hemodynamic parameters in MRI: flow
Evaluation of changes in flow (ml/s) in the Circle of Willis
Improvement of hemodynamic parameters in MRI: endothelial shear stress
Evaluation of changes in endothelial shear stress (Pa) in the Circle of Willis
Full Information
NCT ID
NCT03599609
First Posted
July 2, 2018
Last Updated
October 9, 2020
Sponsor
University of Campinas, Brazil
1. Study Identification
Unique Protocol Identification Number
NCT03599609
Brief Title
Central Nervous System Vascular Changes in Adult Sickle Cell Disease and the Effect of Treatment With Simvastatin
Official Title
Central Nervous System Vascular Changes Evidenced by Magnetic Resonance Imaging in Adult Patients With Sickle Cell Disease and the Effect of Treatment With Simvastatin
Study Type
Interventional
2. Study Status
Record Verification Date
October 2020
Overall Recruitment Status
Unknown status
Study Start Date
March 5, 2018 (Actual)
Primary Completion Date
January 14, 2020 (Actual)
Study Completion Date
July 2021 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Campinas, Brazil
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
5. Study Description
Brief Summary
Stroke is a frequent complication of sickle cell disease (SCD), with varying levels of central nervous system (CNS) involvement. The summation of several ischemic events, even when silent, can lead to devastating consequences, from reduced academic performance to physical dependence. Despite knowledge that brain flow velocities evaluated by Doppler ultrasound identify pediatric SCD patients at a greater stroke risk (Adams et al, NEJM 1998; 339:5-11), this method is not able to predict the occurrence of strokes in adults. There is also no consensus on the management of adult patients in relation to primary and secondary prevention. The aim of this study is to evaluate the effects of the administration of Simvastatin on CNS structural and functional vascular changes in 30 adult patients with SCD (SS and Sβ), above 35 years of age, observed through Magnetic Resonance Imaging (MRI). The data on the effect of simvastatin on disease manifestations is quite scarce, however this drug reportedly significantly reduces plasma concentrations of adhesion molecules and inflammatory markers, such as E-selectin, VEGF, CRP and IL-6 (Hoppe et al, BJH 2011; 153:655-663; Hoppe et al, BJH 2017;177:620-629). Thus, in addition to the search for early diagnostic markers and risk stratification for primary or recurrent stroke, we will also compare CNS images before and 12 months after the administration of Simvastatin. The drug alter stroke recurrence rates in the general adult population, but their effects on vascular changes in patients with SCD have not yet been adequately elucidated. This is particularly important because these are low cost drugs which present good tolerability, and could be part of the therapeutic arsenal of SCD, even in low income settings. Concomitantly with the CNS evaluation, this study also intends to investigate molecular pathways that may be affected by the drugs. We will evaluate microvesicle release patterns, as well as the content of microRNAs possibly involved in the occurrence of stroke, in addition to metabolomic studies and plasma cytokine profile.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Sickle Cell Disease, Stroke
7. Study Design
Primary Purpose
Prevention
Study Phase
Phase 1, Phase 2
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
28 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Treatment
Arm Type
Experimental
Arm Description
Treatment: Simvastatin 40mg/day
Intervention Type
Drug
Intervention Name(s)
Simvastatin 40mg
Intervention Description
Simvastatin 40mg, once daily
Primary Outcome Measure Information:
Title
Stroke prevention
Description
Number of patients in the cohort presenting srtoke or silent infarction detected at MRI
Time Frame
5 years
Secondary Outcome Measure Information:
Title
Improvement of hemodynamic parameters in MRI:velocity
Description
Evaluation of changes in vessel segment-averaged velocity (cm/s) in the Circle of Willis
Time Frame
1 year
Title
Improvement of hemodynamic parameters in MRI: lumen area
Description
Evaluation of changes in vessel lumen area (mm2) in the Circle of Willis
Time Frame
1 year
Title
Improvement of hemodynamic parameters in MRI: flow
Description
Evaluation of changes in flow (ml/s) in the Circle of Willis
Time Frame
1 year
Title
Improvement of hemodynamic parameters in MRI: endothelial shear stress
Description
Evaluation of changes in endothelial shear stress (Pa) in the Circle of Willis
Time Frame
1 year
10. Eligibility
Sex
All
Minimum Age & Unit of Time
35 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Diagnosis of Sickle Cell Disease
Exclusion Criteria:
Previous stroke
Some relevant concomitant clinical condition (cancer, AIDS, inflammatory / autoimmune diseases, etc.).
Pregnancy
Individuals considered to be vulnerable (minors,institutionalized individuals, patients with a history of psychiatric illness with cognitive impairment or incapacity)
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Bruno Benites, MD
Organizational Affiliation
University of Campinas, Brazil
Official's Role
Principal Investigator
Facility Information:
Facility Name
Hematology and Transfusion Medicine Center
City
Campinas
State/Province
São Paulo
ZIP/Postal Code
13083-870
Country
Brazil
12. IPD Sharing Statement
Plan to Share IPD
No
Learn more about this trial
Central Nervous System Vascular Changes in Adult Sickle Cell Disease and the Effect of Treatment With Simvastatin
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