Speech Learning and Speech Production in Parkinson's Disease
NCT07403539
Basal Ganglia Diseases, Behavior
Buffalo, New York, United States
View Trial DetailsNCT Number: NCT06937034
Main objective of this study is to describe the evolution of infusion settings (base, high and low infusion rates) of foslevodopa/foscarbidopa subcutaneous infusion (LDp/CDp) at different timepoints in the treatment of advanced Parkinson's disease (aPD) as captured in ONE-CRM.
Interested in participating?
Request Info18 year and older
All sexes
Observational
Medizinische Universitaet Graz /ID# 278569, Graz, Styria, Austria
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Time frame: Through end of optimization period (defined as no additional dose modification for at least 15 days since the last dose modification).
Mean base infusion rate (ml/hour) will be assessed
Time frame: Through end of optimization period (defined as no additional dose modification for at least 15 days since the last dose modification).
Mean low infusion rate (ml/hour) will be assessed
Time frame: Through end of optimization period (defined as no additional dose modification for at least 15 days since the last dose modification).
Mean high infusion rate (ml/hour) will be assessed
Interested in participating?
Request InfoAbbVie
Industry
Observational Retrospective CoHort Study on Practical ExperienceS of Treatment With Foslevodopa/foScaRbidopa in Advanced Parkinson's Disease
Acronym: ORCHESTRA
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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