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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02946905
Other study ID # 12040139
Secondary ID
Status Completed
Phase
First received
Last updated
Start date April 2016
Est. completion date March 31, 2023

Study information

Verified date April 2023
Source University of Pittsburgh
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Cognitive impairment is a poorly understood, serious, and emerging complication for adult patients with sickle cell disease. Because there is extensive microvascular damage from oxidative damage in sickle cell disease, the investigators hypothesize that this is also present in the cerebral microvasculature to cause cognitive impairment. The investigators plan to test this by correlating markers of inflammation and oxidative damage with cognitive performance and 7 Tesla brain MRI microvascular findings in these patients, with the long term goal of understanding the mechanisms and risk factors of cognitive impairment in sickle cell disease.


Description:

The Neurovascular Determinants of Cognitive Function in Adults with Sickle Cell Disease is a study for adults 18 and older who have been diagnosed with Sickle Cell Disease (SCD). Many adult patients with SCD suffer from cognitive impairment (CI), a serious complication responsible for severe functional limitations, and whose pathogenesis, risk factors, and natural history are unknown. This research project will look at cognitive performance and 7 Tesla brain MRI findings along with markers of inflammation and oxidation to better understand the mechanism and risk factors. The investigators will complete a baseline assessment. SCD participants will be seen for follow-up at 3 and 5 years. Non-SCD participants will be seen for follow-up at 3 years. All assessments are completed at no cost and there is compensation for participation.


Recruitment information / eligibility

Status Completed
Enrollment 226
Est. completion date March 31, 2023
Est. primary completion date March 31, 2023
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: 1. Age 18 and above 2. Able to provide informed consent For Non-SCD : 1. Between age 18 and 55 2. Able to provide informed consent 3. Are age, race, and gender matched to a Sickle Cell Disease study subject. Exclusion Criteria: 1. Age less than 18 years 2. Current pregnancy or lactation 3. Any medical condition that may result in neurocognitive or brain dysfunction that is not secondary to SCD including: 1. Diabetes mellitus 2. Coronary artery disease 3. Peripheral vascular disease 4. Other causes of cerebral vasculitis such as Systemic Lupus Erythematosus (SLE) 4. Any contraindication to MRI scanning including: 1. History of claustrophobia 2. Presence of metallic implants such as cardiac pacemaker or implantable defibrillator, surgical aneurysm clips, or any implanted device (e.g. insulin pump, drug infusion device) 3. Any known metal fragments embedded in the body (eg: ear implant) 4. Neural stimulator (e.g. Transcutaneous Electrical Nerve Stimulation Unit) 5. Metal in the eye (e.g. from machining) 6. Any metallic foreign body, shrapnel, or bullet 7. Inability to lie still for 30 minutes or more 5. Inability to provide direct consent 6. In a current medical or pain crisis as diagnosed by attending physician -

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
University of Pittsburgh

Outcome

Type Measure Description Time frame Safety issue
Primary 7 Tesla MRI Multiple conventional and novel markers of small vessel disease will be evaluated. 5 years
Secondary Inflammation Blood biomarkers of inflammation will be collected 5 years
Secondary Oxidative markers Blood biomarkers of oxidative markers will be collected. 5 years
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