Clinical TrialID 4962

A Study to Evaluate the Effects of Tyramine in Patients Who Completed the PRESTO Study.

NCT00203125

Parkinson's Disease

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Record Fields

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Clinical Trial Id
4962
Evidence Id
4962
Core Evidence Id
4962
Source Clinical Trial Id
4942
Herb2 Clinical Trial Id
HBCT004942
Nct Id
NCT00203125
Title
A Study to Evaluate the Effects of Tyramine in Patients Who Completed the PRESTO Study.
Status
Completed
Phase
Phase 3
Study Result
No
Study Condition
Parkinson's Disease
Study Type
Interventional
Study Design
Allocation: RANDOMIZED|Intervention Model: PARALLEL|Masking: DOUBLE (PARTICIPANT, INVESTIGATOR)|Primary Purpose: TREATMENT
Intervention
DRUG: rasagiline mesylate|OTHER: tyramine
Intervention Allocation
Randomized
Intervention Model
Parallel
Intervention Mask
Double
Intervention Purpose
Treatment
Gender
All
Age
Child, Adult, Older_Adult
Enrollment
55
Outcome Measure
An increase in systolic blood pressure of > 30mmHg from the mean baseline value (documented by at least 3 consecutive measurements). Or Bradycardia with a heart rate below 40 beats per minute, 26 weeks
Sponsor Collaborator
Teva Branded Pharmaceutical Products R&D, Inc.
Funded By
INDUSTRY
Location
Other Id
TVP - 1012/133a
Start Date
2000-10
Primary Completion Date
2003-01
Completion Date
2003-01
First Posted
2005-09-20
Results First Posted
Last Update Posted
2011-04-12
Study Document
Study Url
https://clinicaltrials.gov/study/NCT00203125
Title Cn
Title En
A Study to Evaluate the Effects of Tyramine in Patients Who Completed the PRESTO Study.
Bilingual Status
semi_complete