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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00245700
Other study ID # R050017
Secondary ID Grant from Orion
Status Completed
Phase N/A
First received October 27, 2005
Last updated May 22, 2008
Start date April 2005
Est. completion date July 2006

Study information

Verified date May 2008
Source South Glasgow University Hospitals NHS Trust
Contact n/a
Is FDA regulated No
Health authority United Kingdom: Research Ethics Committee
Study type Observational

Clinical Trial Summary

To test if combining two antiparkinson drugs into a single tablet improves accuracy of medicine intake by the patient.

To test if patients with Parkinson's disease who take medicines at regular time intervals have smoother symptom control.


Recruitment information / eligibility

Status Completed
Enrollment 14
Est. completion date July 2006
Est. primary completion date
Accepts healthy volunteers
Gender Both
Age group 18 Years to 85 Years
Eligibility Inclusion Criteria:

- Patients diagnosed with Parkinson's disease aged between 18 and 85 years fulfilling UK Brain Bank criteria.

- Current levodopa therapy prescribed on a regular basis three or more times per day but requiring entacapone because of 'wearing off'

- Able to manipulate electronic monitoring bottles and complete questionnaires

Exclusion Criteria:

- Current use of compliance aid such that study participation would be detrimental to patient's adherence

- Pregnancy or breast feeding

- Excess alcohol (over 21 units per week for women and 28 units for men)

- Mini mental state examination of less than 26.

- Severe depression (Geriatric depression score over 20)

Study Design

N/A


Related Conditions & MeSH terms


Locations

Country Name City State
United Kingdom Southern General Hospital Glasgow Scotland

Sponsors (1)

Lead Sponsor Collaborator
South Glasgow University Hospitals NHS Trust

Country where clinical trial is conducted

United Kingdom, 

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