Trials / Terminated
TerminatedNCT04151446
Safety & Efficacy of the Laser Scleral Microporation Procedure (Taiwan)
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
- 11 (actual)
- Sponsor
- ACE Vision Group, Inc. · Industry
- Sex
- All
- Age
- 45 Years
- Healthy volunteers
- Not 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
| Type | Name | Description |
|---|---|---|
| DEVICE | Laser Scleral Microporation | Partial depth scleral microporations with an Er:YAG laser in a predetermined pattern. |
Timeline
- Start date
- 2019-04-23
- Primary completion
- 2019-12-31
- Completion
- 2019-12-31
- First posted
- 2019-11-05
- Last updated
- 2022-08-03
Locations
2 sites across 1 country: Taiwan
Source: ClinicalTrials.gov record NCT04151446. Inclusion in this directory is not an endorsement.