Ocular comfort was measured using the visual analogue scale of 0 to 100. Where 0 is extremely uncomfortable and 100 is extremely comfortable.
| Group | Value | 95% CI |
|---|---|---|
| Test | 81.96 | ± 12.407 |
| Control | 82.49 | ± 15.238 |
Last reviewed · How we verify
Clinical Evaluation of Two Marketed Artificial Tears in Non-contact Lens Wearing Patients
Phase 4 trial testing Test Eye Drops in Visual Acuity in 57 participants. Completed in 16 May 2018.
| Lead sponsor | Johnson & Johnson Vision Care, Inc. |
|---|---|
| Phase | Phase 4 |
| Status | Completed |
| Study type | INTERVENTIONAL |
| Allocation | randomized |
| Design | crossover |
| Masking | double |
| Primary purpose | treatment |
| Enrollment | 57 |
| Start date | 9 February 2018 |
| Primary completion | 16 May 2018 |
| Estimated completion | 16 May 2018 |
| Sites | 1 location across United Kingdom |
Johnson & Johnson Vision Care, Inc. — full company profile →
Adults 18 to 69, any sex, with Visual Acuity. Patients with the condition only — healthy volunteers not accepted.
Per-arm endpoint measurements with 95% confidence intervals where reported. Source: trial results section.
Ocular comfort was measured using the visual analogue scale of 0 to 100. Where 0 is extremely uncomfortable and 100 is extremely comfortable.
| Group | Value | 95% CI |
|---|---|---|
| Test | 81.96 | ± 12.407 |
| Control | 82.49 | ± 15.238 |
Subjective dryness was assessed using Ocular Surface Disease Index (OSDI©) instrument. Dryness is evaluated on a scale of 0 to 100, where higher scores indicate more symptoms of dryness
| Group | Value | 95% CI |
|---|---|---|
| Test | 25.68 | ± 10.162 |
| Control | 24.69 | ± 10.609 |
This clinical study is a randomized, double-masked, cross-over, bilateral, 2 treatment x 2 period, dispensing 4-visit study with a 7-9 day washout period in between visits 2 and 3. The study will last approximately 3 months.
No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.
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