Viewing Study NCT00431600



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Study NCT ID: NCT00431600
Status: COMPLETED
Last Update Posted: 2018-06-11
First Post: 2007-02-05

Brief Title: The Validity of Retinal Blood Flow Measurements During Hyperoxia in Humans Using Fourier Domain Color Doppler Optical Coherence Tomography CDOCT
Sponsor: Medical University of Vienna
Organization: Medical University of Vienna

Study Overview

Official Title: The Validity of Retinal Blood Flow Measurements During Hyperoxia in Humans Using Fourier Domain CDOCT
Status: COMPLETED
Status Verified Date: 2018-06
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: Noninvasive monitoring of blood flow in retinal circulation may elucidate the progression and treatment of ocular disorders including diabetic retinopathy age-related macular degeneration and glaucoma

Laser Doppler velocimetry LDV a noninvasive optical method combined with vessel size determination has been used extensively as a valuable research tool to examine blood flow dynamics in the human retina However no information on the velocity profile within the vessel is available Ophthalmic color Doppler optical coherence tomography CDOCT provides laser Doppler information in addition to conventional optical coherence tomography allowing the observation of blood flow dynamics simultaneously to imaging retinal structure

We have recently demonstrated the feasibility of Fourier domain CDOCT to assess velocity profiles in human retinal vessels in vivo

In the present study the validity of Fourier domain CDOCT for retinal blood flow measurements will be tested at baseline and during hyperoxia-induced vasoconstriction in humans by comparison with retinal blood flow measurements using a commercially available LDV system and the Zeiss retinal vessel analyzer RVA
Detailed Description: None

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None