18 and older, any sex, with Myopia or Refractive Errors. Patients with the condition only — healthy volunteers not accepted.
Results — posted to ClinicalTrials.gov
Per-arm endpoint measurements with 95% confidence intervals where reported. Source: trial results section.
Monocular Visual Acuity (VA) With Contact Lenses at Each Visit (Snellen)Primary· Dispense, Week 1, Week 2, Month 1, Month 2, Month 3
VA was assessed for each eye individually using a Snellen chart at a distance of 4 meters. A 20/20 Snellen acuity is considered normal distance eyesight. No formal hypotheses were formulated; hence no inferential testing was performed.
Dispense @ 20/15
Group
Value
95% CI
DD T2
74
DT 1
32
Dispense @ 20/20
Group
Value
95% CI
DD T2
62
DT 1
40
Dispense @ 20/25
Group
Value
95% CI
DD T2
2
DT 1
0
Dispense @ 20/30
Group
Value
95% CI
DD T2
0
DT 1
0
Week 1 @ 20/15
Group
Value
95% CI
DD T2
75
DT 1
36
Week 1 @ 20/20
Group
Value
95% CI
DD T2
58
DT 1
36
Week 1 @ 20/25
Group
Value
95% CI
DD T2
4
DT 1
0
Week 1 @ 20/30
Group
Value
95% CI
DD T2
1
DT 1
0
Sponsor's own description
The purpose of this study is to evaluate the performance of the investigational verofilcon A contact lens compared to the commercially available delefilcon A contact lens, by assessing visual acuity as the primary variable.
Publications & conference data
No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.
Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
Sponsor: as reported to ClinicalTrials.gov by Alcon Research
Last refreshed: 22 February 2019
Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT03305770.