Expired Study
This study is not currently recruiting Study Participants on ClinicalConnection.com. If you would like to find active studies please search for clinical trials.

La Jolla, California 92093


Purpose:

The primary objective of this clinical study is to compare the Nidek RS-3000 Optical Coherence Tomography (OCT) device to the Optovue RTVue OCT. The secondary objective is to evaluate any adverse events found during the clinical study.


Criteria:

Inclusion Criteria: 1. Subjects of legal age and who have full legal capacity to volunteer on the date the informed consent is signed. 2. Subjects who follow the instructions by Principal/Clinical Investigator or clinical staff at the clinical site, and can visit on a scheduled examination date. 3. Subjects who sign an informed consent form to participate in the clinical study. 4. Subjects who agree to take the qualifying examination and RS-3000 and RTVue data acquisition. Exclusion Criteria: 1. Diabetes mellitus (DM) and/or diabetic retinopathy 2. Hypertension (HT) 3. Cerebral infarction, cerebral hemorrhage, cranial nerve neoplasm and other central nervous system diseases affecting vision 4. Cardiac, hepatic, renal and hematologic diseases 5. Current systemic administration of steroid 6. History of anticancer agent etc. 7. Optically-stimulated epileptic seizure 8. Dementia 9. Subjects who have other life threatening and debilitating systemic diseases NOTE: Additional detailed inclusion/exclusion ophthalmic criteria dependent upon study population also exist


NCT ID:

NCT01384487


Primary Contact:

Principal Investigator
Robert Weinreb, M.D.
UCSD, Hamilton Glaucoma Center


Backup Contact:

N/A


Location Contact:

La Jolla, California 92093
United States



There is no listed contact information for this specific location.

Site Status: N/A


Data Source: ClinicalTrials.gov

Date Processed: August 31, 2019

Modifications to this listing: Only selected fields are shown, please use the link below to view all information about this clinical trial.


Click to view Full Listing

This study is not currently recruiting Study Participants on ClinicalConnection.com. The form below is not enabled.