N/A
Completed N=92
Clinical Performance Evaluation of Two Frequent Replacement Silicone Hydrogel Toric Contact Lenses
Source: ClinicalTrials.gov NCT05959200 ↗Enrolled (actual)
92
Serious AEs
0.0%
Results posted
Nov 2024
Primary outcomePrimary: Percentage of Lenses With Axis Orientation Within Plus or Minus 30 Degrees From the Intended Axis at 10 Minutes After Lens Insertion — 100.0; 100.0 percentage of lenses
Summary
The primary objective of this study is to evaluate the axis orientation of LID226397 toric contact lenses.
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Percentage of Lenses With Axis Orientation Within Plus or Minus 30 Degrees From the Intended Axis at 10 Minutes After Lens Insertion |
100.0; 100.0 | — |
Eligibility Criteria
Key Inclusion Criteria
- Successful wearers of any commercial soft toric contact lenses (except AOfAHP and daily disposable lenses) in both eyes with at least 3 months wearing experience, with a minimum wearing time of 5 days per week and 10 hours per day.
- Able to be fit with and wear contact lenses within the available range of sphere & cylinder power and axes.
- Best corrected distance visual acuity greater than or equal to 20/25 Snellen (0.10 logMAR) in each eye as determined by manifest refraction at screening.
- Other protocol-defined inclusion criteria may apply.
Key Exclusion Criteria
- Wearing habitual contact lenses in an extended wear modality (routinely sleeping in lenses for at least 1 night per week) over the last 3 months prior to enrollment.
- Habitual AOfAHP contact lens wearers and habitual daily disposable lens wearers (worn within last 3 months).
- Other exclusion criteria may apply.
Data sourced from ClinicalTrials.gov (NCT05959200). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication. Informational only — not medical advice.