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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01753583
Other study ID # OPHT-041112
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date July 23, 2013
Est. completion date March 1, 2016

Study information

Verified date February 2020
Source Medical University of Vienna
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Corneal lesions such as corneal abrasions and corneal infiltrates are common in clinical practice. The current study seeks to investigate whether high-resolution OCT is suitable for imaging of these corneal lesions. The present study has the character of a pilot study and the results are intended to be used to develop a standardized protocol for imaging and analysis of these corneal lesions. Based on this protocol, further studies investigating the pathophysiology of corneal lesions or evaluating therapeutic success can be planned.


Recruitment information / eligibility

Status Completed
Enrollment 4
Est. completion date March 1, 2016
Est. primary completion date March 1, 2016
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Men and women aged over 18 years

- Newly diagnosed corneal abrasion or corneal infiltrate

Exclusion Criteria:

- Recurrent corneal erosion

- Participation in a clinical trial in the previous 3 weeks

- Presence of any abnormalities preventing reliable measurements as judged by the investigator

- Any contraindication for topical application of Novain 0.4% eye drops for topical anesthesia or of Minims-Fluorescein Sodium eye drops for fluorescein staining

- Pregnancy, planned pregnancy or lactating

Study Design


Related Conditions & MeSH terms


Intervention

Device:
Optical Coherence Tomography (OCT)
High-resolution OCT imaging of the cornea
Other:
Slit lamp biomicroscopy
Slit lamp biomicroscopy with fluorescein staining and slit lamp photograph

Locations

Country Name City State
Austria Department of Clinical Pharmacology, Medical University of Vienna Vienna

Sponsors (1)

Lead Sponsor Collaborator
Medical University of Vienna

Country where clinical trial is conducted

Austria, 

Outcome

Type Measure Description Time frame Safety issue
Primary Imaging of corneal abrasions and infiltrates The aim of this pilot study is to investigate whether imaging of these corneal alterations is possible. 1 day
Secondary Size and depth of corneal lesions as assessed with high-resolution OCT The volume and size of corneal lesions or infiltrates will be assessed using a specific software. 1 day
Secondary Slit lamp biomicroscopy with fluorescein staining The volume and size of corneal lesions or infiltrates will be assessed. 1 day
See also
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Terminated NCT00579020 - A Phase II Study of Moxidex Ophthalmic Solution for Treatment of Marginal Corneal Infiltrates Phase 2