Clinical TrialID 3770

Efficacy of Tyrosine in Restless Legs Syndrome

NCT01494766

Restless Legs Syndrome (RLS)

Back to Browse

Relationship Network

Interactive first-hop connections across herbs, ingredients, formulas, targets, diseases, symptoms, syndromes, evidence, and monographs.

Click a node to open it in a new tab
Trial: 1Ingredient: 1Links: 1
Arranging relationship network...

Record Fields

Scalar fields from the final clinical_trial record.

Clinical Trial Id
3770
Evidence Id
3770
Core Evidence Id
3770
Source Clinical Trial Id
3744
Herb2 Clinical Trial Id
HBCT003744
Nct Id
NCT01494766
Title
Efficacy of Tyrosine in Restless Legs Syndrome
Status
Completed
Phase
Study Result
No
Study Condition
Restless Legs Syndrome (RLS)
Study Type
Interventional
Study Design
Allocation: NA|Intervention Model: SINGLE_GROUP|Masking: NONE|Primary Purpose: TREATMENT
Intervention
DIETARY_SUPPLEMENT: L-Tyrosine
Intervention Allocation
Intervention Model
Single_Group
Intervention Mask
Intervention Purpose
Treatment
Gender
All
Age
Adult, Older_Adult
Enrollment
5
Outcome Measure
International RLS Survey Group (IRLSSG20) Score, Use of this survey to be used as a marker for severity of RLS symptoms and therefore efficacy of this medication., 6 weeks
Sponsor Collaborator
Seton Healthcare Family
Funded By
OTHER
Location
Seton Family of Hospitals, Austin, Texas, 78701, United States
Other Id
CR-11-146
Start Date
2012-01
Primary Completion Date
2012-05
Completion Date
2012-11
First Posted
2011-12-19
Results First Posted
Last Update Posted
2017-04-27
Study Document
Study Url
https://clinicaltrials.gov/study/NCT01494766
Title Cn
Title En
Efficacy of Tyrosine in Restless Legs Syndrome
Bilingual Status
semi_complete