Suspended
Correlation Between Retinal Metabolism and the Observation of a Visible Retinal Spontaneous Venous Pulse
What is being collected
Data Collection
Collected from today forward - ProspectiveWho is being recruted
Eye Diseases+3
+ Glaucoma
+ Ocular Hypertension
Over 18 Years
+7 Eligibility Criteria
How is the trial designed
Observational
Study Start: January 2013
Summary
Principal SponsorUniversitaire Ziekenhuizen KU Leuven
Study ContactLuis Pinto, MD, PhDMore contacts
Last updated: May 29, 2015Sourced from a government-validated database.Claim as a partner
Study start date: January 1, 2013
Actual date on which the first participant was enrolled.Visual field examen will be performed. Structural examination of the optic disc (confocal microscopy) will be performed. Spontaneous venous pulsation will be recorded after a one minute fundoscopy observation. Oximetry reading in the non-contact retinal oximetry of the first 3 order retinal vessels
Principal SponsorUniversitaire Ziekenhuizen KU Leuven
Study ContactLuis Pinto, MD, PhDMore contacts
Last updated: May 29, 2015Sourced from a government-validated database.Claim as a partner
Protocol
This section provides details of the study plan, including how the study is designed and what the study is measuring.Design Details
120 patients to be enrolled
Total number of participants that the clinical trial aims to recruit.Eligibility
Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.Conditions
Criteria
Any sex
Biological sex of participants that are eligible to enroll.Over 18 Years
Range of ages for which participants are eligible to join.Healthy volunteers allowed
If individuals who are healthy and do not have the condition being studied can participate.Conditions
Pathology
Eye DiseasesGlaucomaOcular HypertensionOptic Nerve DiseasesGlaucoma, Open-AngleLow Tension Glaucoma
Criteria
3 inclusion criteria required to participate
having no other ocular diseases besides glaucoma
individuals over 18 years old
willing to sign an informed consent and able to comply with the requirements of the study
4 exclusion criteria prevent from participating
eye disease (except glaucoma)
history of ocular trauma
intraocular surgery (except for cataract surgery)
systemic diseases with ocular involvement like diabetes
Study Plan
Find out more about all the medication administered in this study, their detailed description and what they involve.Treatment Groups
Study Objectives
3 intervention groups are designated in this study
This study does not include a placebo group
Treatment Groups
Study Objectives
Primary Objectives
Study Centers
These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.This study has 1 location
Recruiting
SuspendedOne Study Center