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Anticholinergic
Active Group for Drooling (GLYCOPAR Trial)
Phase 2
Waitlist Available
Led By Tiago Mestre, MSc, MD
Research Sponsored by Ottawa Hospital Research Institute
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 90 days
Awards & highlights
GLYCOPAR Trial Summary
Sialorrhea is a frequently occurring problem with detrimental effect on quality of life in 25% of PD patients. Currently, there is no intervention approved for sialorrhea in Parkinsons and evidence is only available for a 30-day effect or less. We hypothesize that glycopyrrolate will have a lasting effect in the reduction of sialorrhea in PD patients.
Eligible Conditions
- Drooling
- Parkinson's Disease
GLYCOPAR Trial Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 90 days
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~90 days
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Mean sialorrhea related-disability at end of treatment (day 90) measured by the patient/caregiver-rated ROMP-saliva.
Secondary outcome measures
Mean score in sialorrhea severity at end of treatment (day 90) measured by the sialorrhea scoring scale
Proportion of participants with a reduction of severity of sialorrhea in at least one point from baseline to end of treatment (day 90), measured by the MDS-UPDRS, item 2.2.
GLYCOPAR Trial Design
2Treatment groups
Active Control
Placebo Group
Group I: Active GroupActive Control1 Intervention
This arm will receive the study drug glycopyrrolate.
Group II: Placebo GroupPlacebo Group1 Intervention
Control arm to receive placebo
Find a Location
Who is running the clinical trial?
Ottawa Hospital Research InstituteLead Sponsor
561 Previous Clinical Trials
2,785,663 Total Patients Enrolled
Tiago Mestre, MSc, MDPrincipal InvestigatorThe Ottawa Hospital
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