Completed
Impact of Topical, Retrobulbar and General Anesthesia in Ocular Blood Flow
What is being collected
Data Collection
Collected from today forward - ProspectiveWho is being recruted
Eye Diseases+1
+ Glaucoma
+ Ocular Hypertension
Over 18 Years
+6 Eligibility Criteria
How is the trial designed
Observational
Study Start: February 2013
Summary
Principal SponsorUniversitaire Ziekenhuizen KU Leuven
Last updated: May 29, 2015
Sourced from a government-validated database.Claim as a partner
Study start date: February 1, 2013
Actual date on which the first participant was enrolled.Ultrasound B-mode scans will be performed before and after the anesthetic procedure Doppler scan will be added to the B-mode ultrasound to register the blood flow pattern of the ophthalmic and central retinal arteries Blood pressure and heart rate will be monitored
Principal SponsorUniversitaire Ziekenhuizen KU Leuven
Last updated: May 29, 2015
Sourced 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
240 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 not allowed
If individuals who are healthy and do not have the condition being studied can participate.Conditions
Pathology
Eye DiseasesGlaucomaOcular HypertensionGlaucoma, Open-Angle
Criteria
2 inclusion criteria required to participate
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
history of ocular trauma
ocular disease other than the one motivating surgery
previous extraocular surgery
systemic diseases with ocular involvement like diabetes or Graves Ophthalmopathy
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
CompletedOne Study Center