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Clinical Trial Details — Status: Withdrawn

Administrative data

NCT number NCT01229488
Other study ID # 1006001474 IND
Secondary ID
Status Withdrawn
Phase N/A
First received October 26, 2010
Last updated March 25, 2015
Start date July 2012
Est. completion date July 2013

Study information

Verified date March 2015
Source Indiana University
Contact n/a
Is FDA regulated No
Health authority United States: Food and Drug Administration
Study type Interventional

Clinical Trial Summary

The purpose of this study is to demonstrate the ability of the OcuMetrics system to measure oxygen on the surface of the eye. Oxygen is important to the health of the cornea. The proposed instrument will take advantage of phosphorescent dyes that are sensitive to oxygen concentrations to monitor oxygen concentrations on the surface of the eye. This will have obvious applications in eye research and contact lens testing.


Recruitment information / eligibility

Status Withdrawn
Enrollment 0
Est. completion date July 2013
Est. primary completion date July 2013
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 18 Years to 60 Years
Eligibility Inclusion Criteria:

Exclusion Criteria:

- contact lens wear in last 6 weeks

- Use of topical drugs

Study Design

Intervention Model: Single Group Assignment, Masking: Single Blind (Subject), Primary Purpose: Basic Science


Related Conditions & MeSH terms


Intervention

Device:
Intervention
Project was withdrawn before starting. There were no interventions

Locations

Country Name City State
United States Indiana University School of Optometry Bloomington Indiana

Sponsors (1)

Lead Sponsor Collaborator
Indiana University

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary oxygen tension measurement by new device is comparable with gold standard, but less variable and faster. 2 weeks No
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