Study Intended to Evaluate the Safety and Effectiveness of a Johnson & Johnson Vision Care Inc, (JJVCI) Contact Lens for Use on an Extended-wear Basis for up to 7 Days (6 Nights).

Johnson & Johnson (J&J)

Status: Completed

Conditions: Myopia

Treatments: Device: etafilcon A; Device: galyfilcon A

Study type: Interventional

Funder types: Industry

Identifiers

NCT00241280

CR-1480

Details and patient eligibility

About

Study in the US intended to evaluate the safety and effectiveness of a Johnson & Johnson Vision Care Inc, (JJVCI) contact lens for use on an extended-wear basis for up to 7 days (6 nights).

Enrollment: 504 patients

Sex: All

Ages: 18+ years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• The subject must be at least 18 years of age.
• The subject must read and sign the statement of informed consent and be provided with a copy of the form.
• Minimum of 7 days of successful lens wear
• Contact lens prescription requiring between -1.00 to -6.00 D spherical power
• Less than 1.00 D of astigmatism in either eye

Exclusion criteria

Trial design

504 participants in 2 patient groups

Control

Active Comparator group

Description:

etafilcon A contact lens being worn 7 days/6 nights.

Treatment:

Device: etafilcon A

Test

Experimental group

Description:

galyfilcon A contact lens being worn 7 days/6 nights.

Treatment:

Device: galyfilcon A