Adherence of Stalevo, Entacapone and Levodopa
Study of Adherence of Stalevo, Entacapone and Levodopa
2 other identifiers
observational
14
1 country
1
Brief 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.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for all trials
Started Apr 2005
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
April 1, 2005
CompletedFirst Submitted
Initial submission to the registry
October 27, 2005
CompletedFirst Posted
Study publicly available on registry
October 28, 2005
CompletedStudy Completion
Last participant's last visit for all outcomes
July 1, 2006
CompletedMay 23, 2008
May 1, 2008
October 27, 2005
May 22, 2008
Conditions
Eligibility Criteria
You may qualify if:
- 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
You may not qualify if:
- 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)
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Southern General Hospital
Glasgow, Scotland, G51 4TF, United Kingdom
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Donald G Grosset, MBChB, MD
Study Design
- Study Type
- observational
- Sponsor Type
- OTHER
Study Record Dates
First Submitted
October 27, 2005
First Posted
October 28, 2005
Study Start
April 1, 2005
Study Completion
July 1, 2006
Last Updated
May 23, 2008
Record last verified: 2008-05