Clinical Trials Directory

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UnknownNCT03858270

Inhibition of α-synuclein Cell-cell Transmission by NMDAR Blocker, Memantine

Status
Unknown
Phase
Phase 3
Study type
Interventional
Enrollment
50 (estimated)
Sponsor
Wayne State University · Academic / Other
Sex
All
Age
45 Years – 85 Years
Healthy volunteers
Accepted

Summary

Lewy Body Dementia (LBD), is the second most common form of dementia after Alzheimer's Disease. Dementia is defined as a serious loss in cognitive ability due to damages or disease in the brain beyond what is normal aging. With Lewy Body Dementia, protein deposits, or Lewy Bodies, accumulate in nerve cells throughout the brain, affecting motor control, memory and thinking. LBD can also form with the progression of Parkinson's disease (PD). PD is a degenerative nervous system disorder that affects movement ability. Using more sensitive MRI imaging techniques the investigators are attempting to see if disease progression can be monitored more closely. At the same time, the study medication Memantine will be compared to a placebo to determine if it can be used to slow the progression of PD. The purpose of this study is to assess if disease progression can be better monitored through brain imaging and if Memantine will help slow disease progression.

Conditions

Interventions

TypeNameDescription
DRUGMemantineMemantine will be started at 10 mg tablet once/day for a week at bedtime. After one week Memantine will be administered at 10 mg tablet twice/day for 51 weeks.
OTHERPlaceboPlacebo will be started at 10 mg tablet once/day for a week at bedtime. After one week Placebo will be administered at 10 mg tablet twice/day for 51 weeks.

Timeline

Start date
2019-04-01
Primary completion
2022-04-01
Completion
2023-07-01
First posted
2019-02-28
Last updated
2020-07-01

Locations

1 site across 1 country: United States

Regulatory

Source: ClinicalTrials.gov record NCT03858270. Inclusion in this directory is not an endorsement.