A Prospective Study to Evaluate the Raindrop Near Vision Inlay in Presbyopic Patients With Treatments to Optimize the Ocular Surface Before Implantation
Status unconfirmed · Phase 4
Conditions studied: Presbyopia
In brief
The objective of this study is to evaluate the Raindrop® Near Vision Inlay for the improvement of near vision in presbyopic patients with treatments to optimize the ocular surface before corneal inlay surgery.
Key facts
- Study ID
- NCT03126877
- Run by
- Whitten Laser Eye
- People needed
- 40
- Starts
- 2017-04-10
- Expected to finish
- 2020-12-01
- Last updated by the study team
- 2017-07-14
Who can join
Age: 41 and older, up to 65. Sex: any. Healthy volunteers: not accepted.
Where it is running
- Whitten Laser Eye — Washington D.C., District of Columbia, United States (enrolling)
Full record on ClinicalTrials.gov
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