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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00532571
Other study ID # CoQ10 with PSP/CBD
Secondary ID
Status Completed
Phase Phase 2/Phase 3
First received
Last updated
Start date January 2004
Est. completion date September 2005

Study information

Verified date June 2018
Source Lahey Clinic
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

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) ).


Recruitment information / eligibility

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.

Study Design


Intervention

Drug:
CoQ10


Locations

Country Name City State
United States Lahey Clinic Burlington Massachusetts

Sponsors (1)

Lead Sponsor Collaborator
Lahey Clinic

Country where clinical trial is conducted

United States, 

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