Clinical Trials Directory

Trials / Terminated

TerminatedNCT05068479

Safety & Efficacy of the Laser Scleral Microporation Procedure

Evaluation of the Safety & Efficacy of the Laser Scleral Microporation Procedure to Restore Visual Function and Range of Accommodation

Status
Terminated
Phase
N/A
Study type
Interventional
Enrollment
38 (actual)
Sponsor
ACE Vision Group, Inc. · Industry
Sex
All
Age
48 Years
Healthy volunteers
Accepted

Summary

A new minimally invasive procedure for treating presbyopia is being evaluated to determine if there is improvement in near and intermediate vision after treatment

Detailed description

This is a prospective, controlled, single-center clinical study to evaluate the safety and efficacy of the Laser Scleral Microporation Procedure. Laser Scleral Microporation Procedure is a treatment to restore visual and accommodative function in presbyopic patients. The subjects are bilaterally treated with the Laser Scleral Microporation procedure.

Conditions

Interventions

TypeNameDescription
DEVICEBilateral Laser Scleral Microporation procedurePartial depth scleral microporations with an Er:YAG laser in a predetermined pattern.

Timeline

Start date
2021-04-29
Primary completion
2023-03-29
Completion
2023-03-29
First posted
2021-10-05
Last updated
2023-10-03

Locations

1 site across 1 country: Panama

Source: ClinicalTrials.gov record NCT05068479. Inclusion in this directory is not an endorsement.