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COMPLETED
NCT06053736
NA

1-Week Dispensing Evaluation of REVIVE™ Toric Soft Contact Lenses

Sponsor: Bausch & Lomb Incorporated

View on ClinicalTrials.gov

Summary

Experienced soft contact lens wearing subjects were enrolled in this 1-week, post-market, bilateral, repeated measures, dispensing study. All subjects were seen for a Screening/Dispensing Visit at which informed consent was obtained and eligibility was assessed. If subjects satisfied all eligibility criteria and none of the exclusion criteria, subjects were fit and dispensed study lenses. If unsuccessful in the dispensed lenses, additional lenses were trialed. Once vision and lens fit were determined to be acceptable, eligible subjects wore study lenses in both eyes for at least 8 hours per day (with the exception of the follow-up visits where the lenses were worn for a minimum of 2 hours), for approximately 1 week (7 days +/-3 days). Measurements were taken at the insertion visit and at the 7-day follow-up visit.

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

INTERVENTIONAL

Enrollment

32

Start Date

2023-10-04

Completion Date

2023-12-15

Last Updated

2026-08-25

Healthy Volunteers

Yes

Interventions

DEVICE

REVIVE Toric Soft Contact Lenses

Subjects wore REVIVE™ Toric soft (hioxifilcon D) contact lenses bilaterally on a daily-wear (8-16 hours/day), planned-replacement basis for approximately 1 week.

Locations (1)

Bausch + Lomb

Rochester, New York, United States