MedPath

Efficacy of stimulation therapy for parienets with Retinitis pigmentasa

Phase 3
Conditions
Transcleral Stimulation.
Hereditary retinal dystrophy
Registration Number
IRCT201401299820N6
Lead Sponsor
Tehran University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
20
Inclusion Criteria

inclusion critria:Age between 18-50 ;RP detection with VA better than 0.05
Exlusion critria:Comorbidity like cataract,diabet,Ocular surface or any ocular surgery

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Visual Acuity. Timepoint: 12 week. Method of measurement: Snellen Chart.
Secondary Outcome Measures
NameTimeMethod
Visual Function. Timepoint: 12 week. Method of measurement: Questionair.
© Copyright 2025. All Rights Reserved by MedPath