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Selective Laser Trabeculoplasty (SLT): Efficacy and Safety Outcomes of Optometrist (OD) Performed SLT
To measure the efficacy and safety outcomes of SLT performed by optometrists.
Participants will undergo a pre-procedure examination in order to record baseline findings and to determine if they meet the inclusion criteria in order to undergo the procedure. Participants will undergo the SLT procedure and will be examined at 1 hour, 1 week and 6 weeks. Follow up examinations will evaluate eye pressure reduction and post-procedure complications. The rate complication post-procedure are typically low.
Age
18 - No limit years
Sex
ALL
Healthy Volunteers
No
Northeastern State University
Tahlequah, Oklahoma, United States
Start Date
August 21, 2019
Primary Completion Date
May 8, 2022
Completion Date
August 30, 2022
Last Updated
September 1, 2022
14
ACTUAL participants
Selective Laser Trabeculoplasty
DEVICE
Lead Sponsor
Northeastern State University
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.
View ClinicalTrials.gov Terms and ConditionsNCT07218796