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NCT05713552 · ClinicalTrials.gov registry record · NA

Evaluation of ACUVUE® OASYS 1-Day for Astigmatism Contact Lenses With Alternative Lidstock

A NA study, sponsored by Johnson & Johnson Vision Care.

Completed
Registry status
NA
Development phase
31
Enrollment target

NCT05713552: Completed NA study, sponsored by Johnson & Johnson Vision Care.

NCT05713552 is a NA study that has completed, run by Johnson & Johnson Vision Care. The registered enrollment target is 31 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (98% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT05713552, a NA study, has completed, sponsored by Johnson & Johnson Vision Care.

COMPLETED
Registry status
NA
Development phase
31 participants
Enrollment target

Study Summary

This will be a single-visit, randomized, double-masked, bilateral wear, non-dispensing, 2-sequence × 2-period crossover study to evaluate subject reported ocular symptoms.

Primary Outcome

Ocular symptoms were assessed using open-ended question. Investigators asked each subject if they experienced any eye symptoms or problems with lens wear when wearing the study lenses. If responded "Yes", then subject characterized each symptom to the following scale for each eye: 0 = Not Applicable or Not Recorded, 1 = Mild and results in little or no interference with lens wear, 2 = Moderate AND/OR occasionally interferes with lens wear, and 3 = Severe AND/OR frequently interferes with lens we

Interventions

  • DEVICE Acuvue Oasys 1 Day for Astigmatism with Legacy lidstock
  • DEVICE Acuvue Oasys 1 Day for Astigmatism with Amcor laminated lidstock

Trial Details

FieldValue
Enrollment Target 31 participants
Start Date 2023-01-30
Est. Completion 2023-02-09
Phase NA
Johnson & Johnson Vision Care

142 total trials

What the finished NCT05713552 record still lists

NCT05713552 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 31 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (98% lower).

The record links to 0 conditions, and to 2 interventions - of which Acuvue Oasys 1 Day for Astigmatism with Legacy lidstock is the first listed.

NCT05713552 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT05713552 about?

NCT05713552 is a clinical study titled "Evaluation of ACUVUE® OASYS 1-Day for Astigmatism Contact Lenses With Alternative Lidstock". This will be a single-visit, randomized, double-masked, bilateral wear, non-dispensing, 2-sequence × 2-period crossover study to evaluate subject reported ocular symptoms.

What is the current status of trial NCT05713552?

This trial is currently completed. It is a NA study. The enrollment target is 31 participants. The study started on 2023-01-30. Estimated completion is 2023-02-09.

What interventions are being tested in trial NCT05713552?

The interventions under investigation include: Acuvue Oasys 1 Day for Astigmatism with Legacy lidstock (DEVICE), Acuvue Oasys 1 Day for Astigmatism with Amcor laminated lidstock (DEVICE).

Who is sponsoring clinical trial NCT05713552?

This trial is sponsored by Johnson & Johnson Vision Care, which has 142 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT05713552's enrollment target sits among peer trials

31 1592nd of 2000 higher than 408 of 2,000 other NA trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT05713552, the US trial registry maintained by the National Library of Medicine. NCT05713552 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.