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Clinical Trial Summary

The purpose of this study was to evaluate the use of resources during titration of Duodopa at home.


Clinical Trial Description

Telemedicine (TM) offers an alternative titration procedure allowing the start of Duodopa infusion at home. The study evaluated the use of resources, measured as the number of contacts and time spent by health care professionals (Duodopa nurse specialists and the study Investigators) and the TM technician, during Duodopa infusion at home. Data was collected from four (4) clinical centers in Sweden. Data collection period for each participant started at the decision to administer Duodopa treatment (Baseline) and ended when the Duodopa titration period was complete. Post-titration, the participants and caregiver were interviewed and the investigators and nurses answered a web based questionnaire on their experiences. ;


Study Design

Time Perspective: Prospective


Related Conditions & MeSH terms


NCT number NCT01956032
Study type Observational
Source AbbVie
Contact
Status Completed
Phase N/A
Start date September 2013
Completion date November 2014

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