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Cerebrovascular Reserve Measurements in Sickle Cell Disease

Cerebrovascular Reserve Measurements in Sickle Cell Disease: an MRI Study

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02824406
Acronym
CRUISE
Enrollment
60
Registered
2016-07-06
Start date
2014-08-31
Completion date
2017-12-31
Last updated
2016-07-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Sickle Cell Disease

Keywords

Sickle Cell Anemia, Cerebrovascular Reserve, Perfusion, Vasculopathy, Magnetic Resonance Imaging

Brief summary

The primary aim of this study is to evaluate MRI-based cerebrovascular reserve (CVR) measurements in adult patients with Sickle Cell Disease (SCD). The primary objective is to assess whether there is a correlation between CVR and silent cerebral infarcts (SCIs).

Detailed description

CVR is hypothesized to be impaired in SCD patients and could account for the white matter hyperintensities seen on MRI in these patients. Cerebral blood flow (CBF) alone is not sufficient to provide insight into the hemodynamic status of the brain. CVR allows us to gain insight into the capacity of the cerebrovasculature to respond to increased CBF. Vasculopathy is common in SCD and the caliber of the vessels can be assessed with 4D Flow MRI in response to actue and chronic changes in the velocity and wall shear stress on the intracranial arteries in the Circle of Willis. This study will be performed as a single center, patient-control, cross-sectional, observational study in patients with steady-state SCD and controls. The investigators expect that patients with impaired CVR will have a greater number and/or volume of SCIs.

Interventions

DRUGAcetazolamide

Acetazolamide is administered to all participants to induce vasodilation, in order to assess the physiologic response on cerebral blood flow.

Sponsors

Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA)
Lead SponsorOTHER

Study design

Observational model
CASE_CONTROL
Time perspective
CROSS_SECTIONAL

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

Patient group: * Sickle cell disease; either homozygous sickle cell disease (HbSS), or HbSβ0 thalassemia * 18 years of age or older * Informed consent Inclusion Criteria Control group: * Similar ethnic background as Patient group * 18 years of age or older * Informed consent

Exclusion criteria

Patient group and Control group: * Inability of the patient to provide informed consent or legally incompetent/incapacitated to do so * Contraindications for MRI, such as pregnancy, claustrophobia or the presence of metal in the body * Sickle cell crisis at the moment of participation * History of cerebral pathology that compromises measurements, such as cerebral palsy, brain tumour,meningitis, overt infarct * Brain surgery performed in the last 3 months * Severe liver, heart or renal dysfunction (clearance \< 10 mL/min) * Allergy to sulphonamide * Breastfeeding * Use of phenytoin, procaine or acetylsacylic acid (Ascal/aspirin) * Risk of hypokalaemia (use of diuretics, primary hyperaldosteronism) * Addison's Disease * Severe asthma or emphysema

Design outcomes

Primary

MeasureTime frameDescription
Cerebrovascular Reserve (CVR) from arterial spin labelling-MRI in patients compared to controls20 minutesCerebral blood flow (CBF mL/100g/min) measurement before, during, and after, an intravenous administration of 16mg/kg acetazolamide. The percentage change in CBF will be used as a measure for CVR (%).

Secondary

MeasureTime frameDescription
Cerebral Metabolic Rate of Oxygen in patients and controls2 minutesOxygen extraction fraction and cerebral blood flow are proportional to the cerebral metabolic rate of oxygen. Using the CBF from the primary outcome, and having measured the T2 of blood (which is dependent on oxygen), we can derive the oxygen extraction fraction, which allows us to calculate the cerebral metabolic rate of oxygen (CMRO2) and compare patients with controls.
Blood markers relating to anemia will be related to MRI findingsThrough study completion, an average of 1 yearHematocrit, hemoglobin, hemolysis, red blood cell count, mean corpuscular hemoglobin concentration.
Velocity in the circle of willis assessed with 4D Flow MRI10 minutesVelocity (m/s) before and after acetazolamide challenge will be used to indicate cerebrovascular reserve and compared between patients and controls
Silent Cerebral Infarct (SCI) on T2-weighted FLAIR MRI10 minutesVolume of SCIs will be assessed in relation to CVR

Countries

Netherlands

Contacts

Primary ContactBJ Biemond
b.j.biemond@amc.uva.nl

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026