Progressive Supranuclear Palsy Clinical Trial
Official title:
Effects of Coenzyme Q10 in PSP and CBD, A Randomized, Placebo-Controlled, Double Blind Cross Over Pilot Study
Verified date | June 2018 |
Source | Lahey Clinic |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
To compare the efficacy, safety and tolerability of Coenzyme Q 10 versus placebo in patients with atypical parkinsonian syndromes corticobasal degeneration (CBD) and progressive supranuclear palsy (PSP) ).
Status | Completed |
Enrollment | 0 |
Est. completion date | September 2005 |
Est. primary completion date | |
Accepts healthy volunteers | No |
Gender | All |
Age group | 40 Years and older |
Eligibility |
Inclusion Criteria: - Patients fulfilling the diagnostic criteria of PSP and CBD (above) and who were diagnosed within the past 5 years - Age > 40 - Subjects receiving anticholinergics, amantadine, dopamine agonists, carbidopa/levodopa, eldepryl, or comtan must be on a stable dose for at least 30 days prior to baseline visit. - Patients agreeable to participate in the study. Exclusion Criteria: - Prior or concurrent therapy with anticholinergics, amantadine,a dopamine agonist,carbidopa/levodopa or comtan within 30 days of the baseline visit. - Parkinsons disease or any other atypical parkinsonism; Parkinsonism due to drugs. - History of pallidotomy, thalamotomy, deep brain stimulation or fetal tissue transplant. - Previous use of coenzyme Q10 within 60 days of the baseline visit. |
Country | Name | City | State |
---|---|---|---|
United States | Lahey Clinic | Burlington | Massachusetts |
Lead Sponsor | Collaborator |
---|---|
Lahey Clinic |
United States,
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