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NCT04980456 · ClinicalTrials.gov registry record · NA

Clinical Assessment of Two Daily Wear Monthly Replacement Soft Silicone Hydrogel Contact Lenses

A NA study, sponsored by Alcon Research.

Completed
Registry status
NA
Development phase
257
Enrollment target

NCT04980456: Completed NA study, sponsored by Alcon Research.

NCT04980456 is a NA study that has completed, run by Alcon Research. The registered enrollment target is 257 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (82% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT04980456, a NA study, has completed, sponsored by Alcon Research.

COMPLETED
Registry status
NA
Development phase
257 participants
Enrollment target

Study Summary

The purpose of this study is to compare the clinical performance of TOTAL30 contact lenses with Biofinity contact lenses over 30 days of daily wear.

Primary Outcome

Distance visual acuity (VA) was assessed with study lenses in place. VA was collected for each eye separately using logarithmic of the Minimum Angle of Resolution (logMAR) charts. A logMAR acuity of 0.0 corresponds to 20/20 Snellen acuity (normal visual acuity), with a negative value denoting better than 20/20 visual acuity.

Interventions

  • DEVICE Comfilcon A contact lenses
  • DEVICE Lehfilcon A contact lenses
  • DEVICE CLEAR CARE

Trial Details

FieldValue
Enrollment Target 257 participants
Start Date 2021-08-05
Est. Completion 2021-11-20
Phase NA
Alcon Research

275 total trials

What the finished NCT04980456 record still lists

NCT04980456 is an interventional study that assigns participants to a tested intervention. The registered 257 participants enrollment target is mid-sized for trials with a published cap, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (82% lower).

The record links to 0 conditions, and to 3 interventions - of which Comfilcon A contact lenses is the first listed.

NCT04980456 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT04980456 about?

NCT04980456 is a clinical study titled "Clinical Assessment of Two Daily Wear Monthly Replacement Soft Silicone Hydrogel Contact Lenses". The purpose of this study is to compare the clinical performance of TOTAL30 contact lenses with Biofinity contact lenses over 30 days of daily wear.

What is the current status of trial NCT04980456?

This trial is currently completed. It is a NA study. The enrollment target is 257 participants. The study started on 2021-08-05. Estimated completion is 2021-11-20.

What interventions are being tested in trial NCT04980456?

The interventions under investigation include: Comfilcon A contact lenses (DEVICE), Lehfilcon A contact lenses (DEVICE), CLEAR CARE (DEVICE).

Who is sponsoring clinical trial NCT04980456?

This trial is sponsored by Alcon Research, which has 275 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT04980456's enrollment target sits among peer trials

257 403rd of 2000 higher than 1,597 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 NCT04980456, the US trial registry maintained by the National Library of Medicine. NCT04980456 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.