Cerebrovascular Accident Clinical Trial
To continue studies on the two major neurological complications of sickle cell disease (SCD): namely, stroke and chronic encephalopathy.
BACKGROUND:
Stroke represents a focal brain insult whereas chronic encephalopathy represents a diffuse
brain disturbance involving cognition and memory. The predisposition to stroke and the
potential for dementia were increasingly apparent from our studies and the work of other
investigators in sickle cell disease. The ontogeny of these two processes required further
study before the mechanisms could be clearly articulated; and a coordinated assessment of
cerebrovascular perfusion was needed to decipher the relationship between focal perfusion
deficits and occlusion of large and small cerebral vessels. 150 subjects were enrolled in
these studies. Improved understanding of the mechanisms underlying these two devastating
neurological complications of SCD should result in prevention or effective treatment.
DESIGN NARRATIVE:
Three hypotheses were tested: (1) clinically-silent cranial magnetic resonance imaging (MRI)
abnormalities represented the minimal expression of the neurovascular diathesis, and were
the harbingers of clinically-overt strokes (study A); (2) sickle cell disease patients who
developed cerebral infarctions had a predisposing risk factor(s) that contributed to this
neurological complication (study B); and (3) sickle cell disease patients developed a
chronic encephalopathy and dementia that was independent of the neurovascular diathesis
(study C). Study A was a prospective evaluation of 50 SCD children aged 6 to 12 years
attempting to identify a subgroup of patients at risk for the development of a
clinically-apparent stroke. These patients were evaluated clinically, and underwent MRI
scan, magnetic resonance angiography (MRA), and single photon emission computerized
tomography (SPECT). Study B represented two studies designed to analyze risk factors for
stroke. The first study was a retrospective case-control analysis of 25 young adults who
suffered one or more strokes. These patients were age-matched to an SCD control group which
had been clinically free of strokes and had MRI, MRA, and SPECT studies. The second study
represented a prospective case-control analysis of children who were being followed in study
A. Study C represented a prospective study of 50 SCD children, and 50 age-matched siblings
or closest available relatives. Annual neurological examinations and neuropsychological
evaluations were performed searching for evidence of chronic encephalopathy and dementia.
The longitudinal study design was necessary to dissect out the subtle variables that
contributed to the cognitive deficits. The study was renewed in FY 1998 to continue through
FY 2004.
Note: Darryl DeVivo was PI on Subproject which began in FY 1988 as a competing renewal. The
total grant began several years prior to that. Dollars for the subproject were estimated at
10% of the total funds awarded each year.
The study completion date listed in this record was obtained from the "End Date" entered in
the Protocol Registration and Results System (PRS) record.
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N/A
Status | Clinical Trial | Phase | |
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Completed |
NCT05477238 -
Oxygen Consumption in Post-stroke Patients During Various Walking Activities Compared to Healthy Controls
|
N/A | |
Completed |
NCT00046293 -
ReoPro and Retavase to Treat Acute Stroke
|
Phase 2 | |
Completed |
NCT04584645 -
A Digital Flu Intervention for People With Cardiovascular Conditions
|
N/A | |
Completed |
NCT01116544 -
Treatment of Chronic Stroke With AMES + EMG Biofeedback
|
N/A | |
Withdrawn |
NCT04991038 -
Clinical Investigation to Compare Safety and Efficacy of DAISE and Stent Retrievers for Thrombectomy In Acute Ischemic Stroke Patients
|
N/A | |
Active, not recruiting |
NCT02563886 -
Electrically Assisted Movement Therapy
|
N/A | |
Recruiting |
NCT02446730 -
Efficacy and Safety of BiomatrixTM Stent and 5mg-Maintenance Dose of Prasugrel in Patients With Acute Coronary Syndrome
|
Phase 4 | |
Completed |
NCT02141932 -
Pocket-size Cardiovascular Ultrasound in Stroke
|
N/A | |
Completed |
NCT01915368 -
Determining Optimal Post-Stroke Exercise (DOSE)
|
N/A | |
Recruiting |
NCT02557737 -
Botulinim Toxin Type A Injections by Different Guidance in Stroke Patients With Spasticity on Upper Extremities
|
Phase 3 | |
Recruiting |
NCT01769326 -
Influence of Timing on Motor Learning
|
N/A | |
Terminated |
NCT01705353 -
The Role of HMGB-1 in Chronic Stroke
|
N/A | |
Completed |
NCT01423201 -
Transient Ischemic Attack (TIA) Triage and Evaluation of Stroke Risk
|
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Completed |
NCT01182818 -
Fabry and Stroke Epidemiological Protocol (FASEP): Risk Factors In Ischemic Stroke Patients With Fabry Disease
|
N/A | |
Completed |
NCT01656876 -
The Effects of Mirror Therapy on Upper Extremity in Stroke Patients
|
N/A | |
Completed |
NCT00542256 -
tDCS and Physical Therapy in Stroke
|
N/A | |
Withdrawn |
NCT00573092 -
Analyzing Gene Regions That May Interact With the Effectiveness of High Blood Pressure Drugs
|
N/A | |
Completed |
NCT00377689 -
Evaluation of an Intervention Program Targeted at Improving Balance and Functional Skills After Stroke
|
Phase 2 | |
Recruiting |
NCT00166751 -
Sonographic Assessment of Laryngeal Elevation
|
N/A | |
Completed |
NCT00125619 -
Internally Versus Externally Guided Body Weight-Supported Treadmill Training (BWSTT) for Locomotor Recovery Post-stroke
|
N/A |