Clinical TrialID 759

Cone Rescue in Retinitis Pigmentosa by the Treatment of Lycium Barbarum

NCT02244996

Retinitis Pigmentosa

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Record Fields

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Clinical Trial Id
759
Evidence Id
759
Core Evidence Id
759
Source Clinical Trial Id
742
Herb2 Clinical Trial Id
HBCT000742
Nct Id
NCT02244996
Title
Cone Rescue in Retinitis Pigmentosa by the Treatment of Lycium Barbarum
Status
Completed
Phase
Study Result
Yes
Study Condition
Retinitis Pigmentosa
Study Type
Interventional
Study Design
Allocation: RANDOMIZED|Intervention Model: PARALLEL|Masking: DOUBLE (PARTICIPANT, INVESTIGATOR)|Primary Purpose: TREATMENT
Intervention
DIETARY_SUPPLEMENT: Lycium Barbarum|DIETARY_SUPPLEMENT: Placebo
Intervention Allocation
Randomized
Intervention Model
Parallel
Intervention Mask
Double
Intervention Purpose
Treatment
Gender
All
Age
Adult, Older_Adult
Enrollment
50
Outcome Measure
ETDRS Visual Acuity (High Contrast), The high contrast visual acuity will be measured at the time point of baseline and 12 months. Visual acuity is to measure the eye's ability to resolve fine detail with full refractive error correction. The change of acuity (sec of arc) between 12-month time point and baseline will be provided to show the effect of interventions. The changes of the treatment group will be compared with the changes of the placebo group to illustrate the treatment effect of Lycium Barbarum., 12 months
Sponsor Collaborator
The Hong Kong Polytechnic University|The University of Hong Kong
Funded By
OTHER
Location
The Hong Kong Polytechnic University, Hong Kong, Hong Kong
Other Id
1121876
Start Date
2014-11
Primary Completion Date
2016-04
Completion Date
2017-11
First Posted
2014-09-19
Results First Posted
2019-01-28
Last Update Posted
2019-02-19
Study Document
Study Url
https://clinicaltrials.gov/study/NCT02244996
Title Cn
Title En
Cone Rescue in Retinitis Pigmentosa by the Treatment of Lycium Barbarum
Bilingual Status
semi_complete