Revive Toric RWE Study
Starting soon
Conditions studied: Astigmatism
In brief
This is a post-market observational clinical investigation. The objective of this observational study is to evaluate the visual performance and HCP satisfaction of REVIVE samfilcon B custom toric contact lenses.
Key facts
- Study ID
- NCT06785194
- Run by
- Bausch & Lomb Incorporated
- People needed
- 30
- Starts
- 2026-05-01
- Expected to finish
- 2026-07-01
- Last updated by the study team
- 2025-11-28
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Be 18 years or older on the date the ICF is signed
- Have the capacity to read, understand, and provide written voluntary informed consent
- Have physiologically normal anterior segments not exhibiting clinically significant biomicroscopy findings
- Have no active ocular disease or allergic conjunctivitis
- Not be using any topical ocular medications
- Be willing and able to follow instructions
- Have signed a statement of informed consent
- Be an experienced soft contact lens wearer (have previously used soft contact lenses)
- Meet the indications per the Instructions for Use (IFU) and have a suitable prescription for treatment with the device
You may not qualify if…
- Is participating in another research study
- Is considered by the Investigator to not be a suitable candidate for participation
- Is not eligible for treatment with the study lens per the IFU (contraindicated)
- Has had previous ocular surgery
- Is taking/using ocular, systemic, or topical medications that, in the Investigator's opinion, could potentially affect ocular physiology or lens/solution performance
Where it is running
- Site 101 — Orange Park, Florida, United States
- Site 102 — Orange Park, Florida, United States
- Site 103 — Canton, Georgia, United States
Full record on ClinicalTrials.gov
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