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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT02279446
Other study ID # 263/13-10-2014
Secondary ID
Status Recruiting
Phase N/A
First received October 13, 2014
Last updated October 29, 2014
Start date October 2014
Est. completion date April 2015

Study information

Verified date October 2014
Source Democritus University of Thrace
Contact Georgios Labiris, MD, PhD
Phone 00302551039891
Email labiris@usa.net
Is FDA regulated No
Health authority Greece: Ethics Committee
Study type Observational

Clinical Trial Summary

Development of a validated computer-based instrument (software program) for the assessment of intermediate visual acuity.


Description:

Development of a validated computer-based instrument (software program) for the assessment of intermediate visual acuity (IVA). It is known that no validated method for the evaluation of IVA exists.

Primary objective of the study is to validate a specific computer-based chart (optotype) that will enable: a) comparative studies among different groups of presbyopic patients with refractive errors (ie. myopia, hyperopia, and/or astigmatism), and, b) assessment of the efficacy of surgical refractive procedures (ie. LASIK) on presbyopic patients.

Intermediate Visual acuity chart is similar to the prevalent Jaeger chart. It consists of short blocks of text in various type sizes.The computer screen is set at a specific reading distance (1 meter) and the patient is asked to read the passage with the smallest type he/she can see. According to the smallest text he/she can read, IVA is classified from IVA1 (which is considered the equivalent of 20/20 distance visual acuity) to IVA5

Validation of the computer-based IVA chart will be done by correlating the results of the IVA chart to the corresponding ones from the validated 20/20 distant and Jaeger near visual acuity charts, in a random sample of study participants with different refractive errors and different near and distant visual acuities.


Recruitment information / eligibility

Status Recruiting
Enrollment 400
Est. completion date April 2015
Est. primary completion date October 2014
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- native Greek participants or foreigners with perfect knowledge (verbal and written) of Greek language

Exclusion Criteria:

- glaucoma or suspicion for glaucoma,

- corneal disease or suspicion for corneal disease

- fundus disease or suspicion for fundus disease

- pregnancy or nursing,

- underlying autoimmune disease

- mental or neurologic disease

Study Design

Time Perspective: Cross-Sectional


Related Conditions & MeSH terms


Intervention

Other:
Intermediate Visual acuity (IVA) assessment
Intermediate visual acuity (IVA) will be assessed with the Intermediate Visual acuity chart which is similar to the prevalent Jaeger chart. It consists of short blocks of text in various type sizes.The computer screen is set at a specific reading distance (1 meter) and the patient is asked to read the passage with the smallest type he/she can see. According to the smallest text he/she can read, IVA is classified from IVA1 (which is considered the equivalent of 20/20 distance visual acuity) to IVA5

Locations

Country Name City State
Greece Eye Institute Of thrace Alexandroupolis Evros

Sponsors (1)

Lead Sponsor Collaborator
Democritus University of Thrace

Country where clinical trial is conducted

Greece, 

Outcome

Type Measure Description Time frame Safety issue
Primary Intermediate Visual Acuity (IVA) Number of participants that their intermediate visual acuity measured with the "intermediate visual acuity chart" will be statistically correlated with distant visual acuity (measured by 20/20 chart) and near visual acuity (measured by Jaeger chart) 6 months No
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