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A Multi-center, Randomised, Open-label Study to Evaluate Convenience and Safety of Change in the Mode of Administration of Rivastigmine (From Capsules to a Transdermal Patch) in Patients With Alzheimer's Disease
This study used two doses of rivastigmine transdermal patch (5 cm\^2, 10 cm\^2) to establish the feasibility of 2 switch schedules (with transdermal patch one-step dose titration or without dose titration) from rivastigmine capsules (3 mg bid (bis in die, twice a day), 4,5 mg bid, 6 mg bid) to rivastigmine transdermal patch and to assess safety, tolerability, convenience, and caregivers preferences of rivastigmine transdermal patch versus capsules.
Age
60 - No limit years
Sex
ALL
Healthy Volunteers
No
Novartis Investigative Site
Barcelona, Spain
Start Date
September 1, 2007
Primary Completion Date
April 1, 2009
Completion Date
April 1, 2009
Last Updated
March 24, 2011
142
ACTUAL participants
Rivastigmine patch (4.6 mg/day switch to 9.5 mg/day)
DRUG
Rivastigmine patch (9.5 mg/day)
DRUG
Rivastigmine capsules (6 mg to 12 mg/day)
DRUG
Lead Sponsor
Novartis
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.
View ClinicalTrials.gov Terms and ConditionsNCT07033494