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NCT05114564 · ClinicalTrials.gov registry record · NA

Evaluation of the Performance of Monthly Replacement Sphere Lens Designs in Habitual Soft Contact Lens Wearers

A NA study, sponsored by CooperVision.

Completed
Registry status
NA
Development phase
66
Enrollment target

NCT05114564: Completed NA study, sponsored by CooperVision.

NCT05114564 is a NA study that has completed, run by CooperVision. The registered enrollment target is 66 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (95% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT05114564, a NA study, has completed, sponsored by CooperVision.

COMPLETED
Registry status
NA
Development phase
66 participants
Enrollment target

Study Summary

The objective of the study is to evaluate the clinical performance of two monthly silicone hydrogel contact lenses in habitual wearers of frequent replacement (FRP) lenses when worn for one month.

Primary Outcome

Subjective Ratings on Lens handling on removal (0-10 scale, 0.5 steps; 10=very easy, 0=very difficult)

Interventions

  • DEVICE Lens A (comfilcon A lens)
  • DEVICE Lens B (lehfilcon A lens)

Trial Details

FieldValue
Enrollment Target 66 participants
Start Date 2021-11-19
Est. Completion 2022-04-22
Phase NA
CooperVision

64 total trials

What the finished NCT05114564 record still lists

NCT05114564 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 66 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (95% lower).

The record links to 0 conditions, and to 2 interventions - of which Lens A (comfilcon A lens) is the first listed.

NCT05114564 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT05114564 about?

NCT05114564 is a clinical study titled "Evaluation of the Performance of Monthly Replacement Sphere Lens Designs in Habitual Soft Contact Lens Wearers". The objective of the study is to evaluate the clinical performance of two monthly silicone hydrogel contact lenses in habitual wearers of frequent replacement (FRP) lenses when worn for one month.

What is the current status of trial NCT05114564?

This trial is currently completed. It is a NA study. The enrollment target is 66 participants. The study started on 2021-11-19. Estimated completion is 2022-04-22.

What interventions are being tested in trial NCT05114564?

The interventions under investigation include: Lens A (comfilcon A lens) (DEVICE), Lens B (lehfilcon A lens) (DEVICE).

Who is sponsoring clinical trial NCT05114564?

This trial is sponsored by CooperVision, which has 64 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT05114564's enrollment target sits among peer trials

66 1139th of 2000 higher than 857 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 NCT05114564, the US trial registry maintained by the National Library of Medicine. NCT05114564 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.