RP Cure Tracker

Trials / NCT02244996

Cone Rescue in Retinitis Pigmentosa by the Treatment of Lycium Barbarum

Completed N/A Other

Sponsor
The Hong Kong Polytechnic University
Treatment
Lycium Barbarum; Placebo
Gene
Not stated
Conditions
Retinitis Pigmentosa
Ages
18 Years to 70 Years
Enrollment
50 participants
Started
2014-11
Main results expected
2016-04
Results posted
Yes
Record last updated
2019-02-19

What the study is testing

Objectives: To study the immediate effect and the persistent effect of Lycium barbarum (LB) treatment on retinal functions, especially the cone function, and retinal structure in patients with retinitis pigmentosa (RP) Design: Randomised controlled double-masked trial

Setting: Primary Care clinical trial

Participants: 120 RP subjects will be recruited from Ophthalmology department at The University of Hong Kong and the Retina Hong Kong. Interventions: Subjects will be randomly allocated to LB (treated with LB granules) or control (treated with placebo) groups for 1 year. After the 1st year, both groups will stop the treatment and all subjects will also have the same eye exam in 6-month period for the 2nd year.

Main outcome measures: The primary outcome is the total sensitivity scores of 30-2 \& 60-4 programmes of Humphrey Visual Field Analysis (HVFA). The secondary outcomes are the b-wave amplitudes of Full-field Electroretinogram (ffERG) responses, the amplitudes of direct component and induced component of Multifocal Electroretinogram (mfERG), and the ETDRS visual acuity.

Where it runs

Hong Kong (1)

Open on ClinicalTrials.gov for contacts and eligibility