Clinical and Genetic Characterization of Individuals With Achromatopsia

Status

Completed

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT01846052

Enrollment

Registered

2013-05-03

Start date

2013-06-30

Completion date

2017-04-30

Last updated

2017-10-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Achromatopsia

Keywords

achromatopsia, CNGB3

Brief summary

The purpose of this study is to identify individuals with achromatopsia caused by mutations in the CNGB3 gene and characterize their clinical condition using several tests of visual function every 6 months for up to 1.5 years.

Detailed description

Individuals with a clinical diagnosis of achromatopsia will be asked to provide informed consent and will then have a single 5 mL blood sample drawn for DNA sequence analysis of genes known to cause achromatopsia, including the CNGB3 gene. All participants will be informed of the results of testing for these mutations. Those with mutations in both alleles of the CNGB3 gene will be evaluated every 6 months for up to 1.5 years by using a variety of non-invasive visual function tests to more fully characterize their clinical condition. This testing will include routine ophthalmic examination and tests of visual acuity, color vision, reading speed, perimetry, nystagmus, light sensitivity, optical coherence tomography, adaptive optics retinal imaging, electroretinography, fundus photography and completion of a quality of life questionnaire.

Interventions

None listed

Study design

Observational model

COHORT

Time perspective

PROSPECTIVE

Eligibility

Sex/Gender

ALL

Age

6 Years to No maximum

Healthy volunteers

Inclusion criteria

1. Clinical diagnosis of achromatopsia (screening portion of study); 2. Molecular confirmation of mutations in the CNGB3 gene (main portion of study); 3. At least 6 years of age; 4. Willing and able to perform study procedures; 5. Signed informed consent(s) obtained (and child assent where applicable).

Exclusion criteria

1. Not able to have a blood sample drawn; 2. Pre-existing eye conditions that would interfere with interpretation of study endpoints (e.g. glaucoma, corneal or lenticular opacities, diabetic retinopathy, history of retinal detachment); 3. Participating in an interventional research study of drugs or devices for treatment of achromatopsia or other retinal diseases; 4. Use of medications that may impair color vision (e.g. hydroxychloroquine); 5. Any condition which leads the investigator to believe that the participant cannot comply with the protocol requirements or that may place the participant at an unacceptable risk for participation.

Design outcomes

Primary

Measure	Time frame	Description
Visual acuity	Annually for up to 1.5 years	Visual acuity will be measured by EVA or ETDRS methods

Secondary

Measure	Time frame	Description
Color Vision	annually for up to 1.5 years	Color vision will be measured by Farnsworth D-15 test and anomaloscope
Adaptive Optics Retinal Imaging	annually for up to 1.5 years	Adaptive optics retinal imaging will be performed using the method of Genead et al. (Invest Ophthalmol Vis Sci 2011;52:7298-308).

Countries

United States

Outcome results