Clinical Trial

5-HT RBD REM Sleep Behavior Disorder

Active, Not Recruiting
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Summary
This project will test the hypotheses that people with 5-HT RBD have systemic alpha- synuclein pathology, prodromal DLB signs, and brainstem lesions in regions that control REM sleep. AIM 1 will seek to detect abnormally phosphorylated alpha- synuclein aggregates on targeted skin biopsy in a cohort of people with 5-HT RBD and matched controls (taking SSRIs but without RBD). Aim 2 will use ultra-high field MRI at 7T to examine the pontine region of the coeruleus/subcoeruleus complex for evidence of neurodegeneration as well as segment and parcellate REM sleep related neuronal structures. Aim 3 will test for speech deficits. While these aims are independent we suspect that the severity of autonomic, speech and cognitive deficits will correlate with loss of neuromelanin signal on MRI and pathology on skin biopsy. The investigation is a longitudinal designed study to examine histopathology, neuroimaging changes and speech function from baseline (Time 1) to a follow-up after 30 months (Time 2). A total of 60 individuals, 30 with 5-HT RBD and 30 controls, will be recruited at Time 1, brought back at Time 2, and tested across all Aims at both study visits.
Protocol Amendment History 2 changes
critical Enrollment closed, study ongoing 2026-08-11
notable Enrollment increased: 60 -> 66 participants 2026-08-11
Trial Details
NCT Number NCT06467461
Lead Sponsor University of Minnesota
Conditions Dementia With Lewy Bodies, Parkinson Disease, REM Sleep Behavior Disorder
Enrollment 66 participants
Start Date 2024-02-08
Primary Completion 2027-12-01 (estimated)
Study Completion 2028-09-01 (estimated)
Updated on ClinicalTrials.gov 2026-08-10