The Use of Transcranial Focused Ultrasound for the Treatment of Neurodegenerative Dementias
Status unconfirmed · Not applicable
Conditions studied: Mild Cognitive Impairment, Mild Dementia, Parkinson Disease, Alzheimer Disease
In brief
The purpose of this open label study is to evaluate longer term tolerability and early efficacy of transcranial ultrasound in the treatment of patients with mild cognitive impairment or dementia.
Key facts
- Study ID
- NCT04250376
- Run by
- Neurological Associates of West Los Angeles
- People needed
- 100
- Starts
- 2017-11-27
- Expected to finish
- 2025-01-01
- Last updated by the study team
- 2023-03-24
Who can join
Age: 45 and older, up to 93. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- CDR stage of at least 0.5 (mild cognitive impairment)
- At least one pathognomic imaging biomarker of a neurodegenerative process.
You may not qualify if…
- Cognitive decline clearly related to an acute illness
- Subjects unable to give informed consent
- Subjects with scalp rash or open wounds on the scalp (for example from treatment of squamous cell cancer)
- Advanced terminal illness
- Advanced kidney, pulmonary, cardiac or liver failure
- Subjects who would not be able to lay down without excessive movement in a calm environment sufficiently long enough to be able to achieve sleep
- Subjects with major depressive disorder
- Subjects with vascular causes of dementia
Where it is running
- Neurological Associates of West LA — Santa Monica, California, United States
Full record on ClinicalTrials.gov
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