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Clinical Trial Details — Status: Terminated

Administrative data

NCT number NCT02382627
Other study ID # 14-2348
Secondary ID
Status Terminated
Phase
First received
Last updated
Start date March 2015
Est. completion date December 2018

Study information

Verified date October 2019
Source University of Colorado, Denver
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

This study plans to learn more about the thickness of the choroid in patients with optic neuropathy. The choroid is a layer of blood vessels that supplies oxygen and nourishment to the outer layers of the retina. Patients are being asked to be in this research study because they have optic neuropathy and are receiving care at the University of Colorado Hospital.


Recruitment information / eligibility

Status Terminated
Enrollment 2
Est. completion date December 2018
Est. primary completion date December 2018
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion criteria:

- age greater than 18 years,

- diagnosis of optic neuropathy,

- willing and able to sign an informed consent.

Exclusion criteria:

- steroid use within the past 4 weeks,

- inability to cooperate with optical coherence tomography (OCT) testing,

- relevant ocular comorbidities in the affected or unaffected eye, such as

- glaucoma,

- uveitis,

- optic nerve hypoplasia,

- age related macular degeneration,

- refractive error greater than 5 spherical diopters.

Study Design


Locations

Country Name City State
United States University of Colorado Hospital Aurora Colorado

Sponsors (1)

Lead Sponsor Collaborator
University of Colorado, Denver

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Difference of the subfoveal and parafoveal choroidal thickness in affected and unaffected eye of the same patient. 1 time