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Retina Projection System Trials for Low Vision People
This study has been completed.
First Received: September 14, 2005   Last Updated: May 20, 2008   History of Changes
Sponsors and Collaborators: Osaka City University
Nihon University Surugadai Hospital
Kurume University
Miyata Eye Hospital
Fukuoka Kinen Hospital
Kimura Eye and Medical Hospital
Information provided by: Osaka City University
ClinicalTrials.gov Identifier: NCT00219427
  Purpose
  1. Purpose

    a. Examination on Efficacy of Retina Projection System

  2. Patients

    a. Low vision patients

  3. Methods

    1. Vision aids

      • Retina Projection System
      • Face-mounted video display as control
    2. Comparison of Reading Speeds with both vision aids

Condition
Vision, Low

Study Type: Observational
Study Design: Case-Only, Prospective
Official Title: Multicenter Clinical Trials of Retina Projection System

Further study details as provided by Osaka City University:

Primary Outcome Measures:
  • Reading speeds with two different vision aids [ Time Frame: Visits for measuring reading speeds ] [ Designated as safety issue: No ]

Biospecimen Retention:   None Retained

Biospecimen Description:

Enrollment: 58
Study Start Date: January 2005
Study Completion Date: December 2005
Primary Completion Date: November 2005 (Final data collection date for primary outcome measure)
Groups/Cohorts
1

Detailed Description:
  1. Purpose

    a. Examination on efficacy of a new vision aid of Retina Projection System

  2. Patients

    1. Low vision patients
    2. Vision between 0.06 and 0.3
    3. no exclusion on kinds of ocular diseases
  3. Methods

    1. Vision aids

      • Retina Projection System
      • Face-mounted video display as control
    2. Computer-aided measurement of reading speeds of individual characters
    3. Comparison of reading Speeds with the two vision aids
  Eligibility

Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Sampling Method:   Non-Probability Sample
Study Population

primary care clinic

Criteria

Inclusion Criteria:

  • low vision patients
  • vision between 0.06 and 0.3

Exclusion Criteria:

  • light perception
  • hand motion
  • vision less than 0.06
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00219427

Locations
Japan
Fukuoka Kinen Hospital
Fukuoka, Japan, 814-8525
Osaka City University
Osaka, Japan, 545-8585
Nihon University Surugadai Hospital
Tokyo, Japan, 101-8309
Japan, Fukuoka
Kurume University
Kurume, Fukuoka, Japan, 830-0011
Japan, Hiroshima
Kimura Eye and Medical Hospital
Kure, Hiroshima, Japan, 737-0046
Japan, Miyazaki
Miyata Eye Hospital
Miyakonojo, Miyazaki, Japan, 885-0051
Sponsors and Collaborators
Osaka City University
Nihon University Surugadai Hospital
Kurume University
Miyata Eye Hospital
Fukuoka Kinen Hospital
Kimura Eye and Medical Hospital
Investigators
Study Director: Kunihiko Shiraki, MD Dept. of Ophthalmology and Visual Sciences, Osaka City University, Graduate School of Medicine
  More Information

No publications provided

Responsible Party: Osaka City University, Dept of Ophthalmology ( Kunihiko Shiraki, MD )
Study ID Numbers: OCUM2004681, OCUM2004681
Study First Received: September 14, 2005
Last Updated: May 20, 2008
ClinicalTrials.gov Identifier: NCT00219427     History of Changes
Health Authority: Japan: Ministry of Health, Labor and Welfare

Keywords provided by Osaka City University:
Low vision

Study placed in the following topic categories:
Signs and Symptoms
Sensation Disorders
Vision Disorders
Eye Diseases
Neurologic Manifestations
Vision, Low

Additional relevant MeSH terms:
Signs and Symptoms
Sensation Disorders
Vision Disorders
Eye Diseases
Nervous System Diseases
Neurologic Manifestations
Vision, Low

ClinicalTrials.gov processed this record on September 01, 2009