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NCT01952665 · ClinicalTrials.gov registry record · NA

A Multi-Center Study Comparing the Clinical Performance of Two Silicone Hydrogel Lenses Over 1 Month of Daily Wear

A NA study, sponsored by CooperVision.

Completed
Registry status
NA
Development phase
63
Enrollment target

NCT01952665: Completed NA study, sponsored by CooperVision.

NCT01952665 is a NA study that has completed, run by CooperVision. The registered enrollment target is 63 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

NCT01952665, a NA study, has completed, sponsored by CooperVision.

COMPLETED
Registry status
NA
Development phase
63 participants
Enrollment target

Study Summary

A Multi-Center Study Comparing the Clinical Performance of Two Silicone Hydrogel Lenses Over 1 Month of Daily Wear

Primary Outcome

Participant rating for lens comfort on insertion. Collected at dispense for both study lens pairs. (0-10, 0= Very Uncomfortable, 10= Cannot feel).

Interventions

  • DEVICE lotrafilcon B
  • DEVICE comfilcon A

Trial Details

FieldValue
Enrollment Target 63 participants
Start Date 2013-10
Est. Completion 2014-03
Phase NA
CooperVision

64 total trials

What the finished NCT01952665 record still lists

NCT01952665 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 63 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 lotrafilcon B is the first listed.

NCT01952665 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01952665 about?

NCT01952665 is a clinical study titled "A Multi-Center Study Comparing the Clinical Performance of Two Silicone Hydrogel Lenses Over 1 Month of Daily Wear". A Multi-Center Study Comparing the Clinical Performance of Two Silicone Hydrogel Lenses Over 1 Month of Daily Wear

What is the current status of trial NCT01952665?

This trial is currently completed. It is a NA study. The enrollment target is 63 participants. The study started on 2013-10. Estimated completion is 2014-03.

What interventions are being tested in trial NCT01952665?

The interventions under investigation include: lotrafilcon B (DEVICE), comfilcon A (DEVICE).

Who is sponsoring clinical trial NCT01952665?

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

How this trial's enrollment target compares

Where NCT01952665's enrollment target sits among peer trials

63 1157th of 2000 higher than 844 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 NCT01952665, the US trial registry maintained by the National Library of Medicine. NCT01952665 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.