NCT01952665

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

• Status: Completed
• Phase: N/A
• Study type: Interventional
• Enrollment: 63 (actual)
• Sponsor: CooperVision, Inc. · Industry
• Sex: All
• Age: 18 Years – 40 Years
• Healthy volunteers: Not accepted

Summary

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

Detailed description

Two-month, single masked, randomized, bilateral, crossover, 1-month of daily wear in each study lens.

Conditions

• Myopia

Interventions

Type	Name	Description
DEVICE	comfilcon A	Each subject randomized to wear the test lens (comfilcon A) or the control lens (lotrafilcon B) for one month of daily wear before repeating schedule for the second pair without a washout period.
DEVICE	lotrafilcon B	Each subject randomized to wear the test lens (comfilcon A) or the control lens (lotrafilcon B) for one month of daily wear before repeating schedule for the second pair without a washout period.

Timeline

• Start date: 2013-10-01
• Primary completion: 2013-11-01
• Completion: 2014-03-01
• First posted: 2013-09-30
• Last updated: 2017-06-26
• Results posted: 2015-09-24

Locations

6 sites across 1 country: United States