N/A
Completed N=40
A Clinical Comparison of Two Soft Toric Contact Lenses
Astigmatism
Source: ClinicalTrials.gov NCT06758089 ↗
Enrolled (actual)
40
Serious AEs
0.0%
Results posted
Feb 2026
Primary outcomePrimary: Subjective Overall Score — 76.5; 75.5 units on a scale
Summary
The aim of this study is to compare the short-term clinical performance of two toric contact lenses.
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Subjective Overall Score |
76.5; 75.5 | — |
| SECONDARY Subjective Vision |
78.9; 73.8 | — |
| SECONDARY Subjective Comfort |
80.1; 82.3 | — |
Eligibility Criteria
Inclusion Criteria
- They are of legal age and capacity to volunteer.
- They understand their rights as a research subject and are willing and able to sign a Statement of Informed Consent.
- They are willing and able to follow the protocol.
- They currently wear soft contact lenses, or have done so within the past two years.
- They have ocular astigmatism in both eyes of between 0.75DC and 2.00DC.
- They have a spherical component: plano to -7.00DS (based on ocular refraction).
- They are expected to be able to be fitted with the study lenses within the power range available.
Exclusion Criteria
- They have an ocular disorder, which would normally contra-indicate contact lens wear.
- They have a systemic disorder, which would normally contra-indicate contact lens wear.
- They are using any topical medication such as eye drops or ointment.
- They are aphakic.
- They have had corneal refractive surgery.
- They have any corneal distortion resulting from previous hard or rigid lens wear or have keratoconus.
- They are pregnant or breastfeeding.
- They have an eye or health condition including an immunosuppressive or infectious disease which would, in the opinion of the investigator, contraindicate contact lens wear or pose a risk to study personnel; or a history of anaphylaxis or severe allergic reaction.
- They have taken part in any contact lens or care system clinical research within two weeks prior to starting this study.
Data sourced from ClinicalTrials.gov (NCT06758089). 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.