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NCT01706770 · ClinicalTrials.gov registry record · NA

Evaluation of Enfilcon A Soft Contact Lens When Compared to Galyfilcon A Soft Contact Lens

A NA study, sponsored by CooperVision.

Completed
Registry status
NA
Development phase
50
Enrollment target

NCT01706770: Completed NA study, sponsored by CooperVision.

NCT01706770 is a NA study that has completed, run by CooperVision. The registered enrollment target is 50 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (96% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT01706770, a NA study, has completed, sponsored by CooperVision.

COMPLETED
Registry status
NA
Development phase
50 participants
Enrollment target

Study Summary

The primary objective of thes study is to confirm that the ocular response to the Test lenses are similar to those of the Control lenses when used in a 1 week planned replacement, daily wear modality over a 1-month period.

Primary Outcome

The primary safety endpoint are the objective slit lamp findings associated with the enfilcon A contact lenses compared with those same findings reported as associated with the galyfilcon A contact lenses. The incidence of biomicroscopy findings (0=not present, 4=severe) over the duration of the study with the highest reported grade was chosen for each unique eye. Biomicroscopy measurements were obtained at Baseline/Dispensing (baseline and dispensing visit combined), Post-Dispensing (after len

Interventions

  • DEVICE enfilcon A
  • DEVICE galyfilcon A

Trial Details

FieldValue
Enrollment Target 50 participants
Start Date 2012-05
Est. Completion 2012-10
Phase NA
CooperVision

64 total trials

What the finished NCT01706770 record still lists

NCT01706770 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 50 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (96% lower).

The record links to 0 conditions, and to 2 interventions - of which enfilcon A is the first listed.

NCT01706770 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01706770 about?

NCT01706770 is a clinical study titled "Evaluation of Enfilcon A Soft Contact Lens When Compared to Galyfilcon A Soft Contact Lens". The primary objective of thes study is to confirm that the ocular response to the Test lenses are similar to those of the Control lenses when used in a 1 week planned replacement, daily wear modality over a 1-month period.

What is the current status of trial NCT01706770?

This trial is currently completed. It is a NA study. The enrollment target is 50 participants. The study started on 2012-05. Estimated completion is 2012-10.

What interventions are being tested in trial NCT01706770?

The interventions under investigation include: enfilcon A (DEVICE), galyfilcon A (DEVICE).

Who is sponsoring clinical trial NCT01706770?

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

How this trial's enrollment target compares

Where NCT01706770's enrollment target sits among peer trials

50 1279th of 2000 higher than 622 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 NCT01706770, the US trial registry maintained by the National Library of Medicine. NCT01706770 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.