Clinical Evaluation of Investigational Contact Lenses

NCT02801396 | Completed Results FDA Device

• 1 other identifier: CR-5759
• Study Type: interventional
• Target: 116
• Locations: 1 country
• Sites: 1

Brief Summary

Single-visit, unmasked, non-dispensing study where subjects will wear three different lenses bilaterally in one visit, each lens being worn for approximately 30-60 minutes. Subjects will complete a questionnaire for each study lens.

Conditions

Visual Acuity

Outcome Measures

Primary Outcomes (4)

• CLUE Handling

  CLUE Handling is assessed using the Contact Lens User Experience (CLUE™) Questionnaire. CLUE™ is a validated patient-reported outcomes questionnaire to assess patient experience attributes of soft, disposable contact lenses (comfort, vision, handling, and packaging) in a contact lens-wearing population in the US, ages 18-65. Scores follow a normal distribution with a population average score of 60 (SD 20), where higher scores indicate a more favorable / positive response. 97% of the scores fall within 0 and 120 (mean +/- 3XSD).

  30 Minutes Post Insertion

• Visual Performance (LogMar)

  Distance time controlled Visual Performance (LogMAR) was assessed for each subject eye under bright-illumination high-contrast lighting conditions at 4m using an ETDRS chart. The average visual performance (LogMAR) was reported for each study lens.

  30 Minutes Post Insertion

• Percentage of Eyes With Acceptable Mechanical Lens Fit

  Mechanical lens fit will be assessed for each subject and eye using a slit lamp. Lens fit is a binary response and 'Yes' = Acceptable Fit and 'No' = Unacceptable Fit. Lens fit is assessed using Lens centration, limbal exposure, primary gaze movement, up-gaze movement, edge lift, lens tightness. Unacceptable fit will be declared if there is any of the following present: limbal exposure, edge lift, excessive movement in primary or up-gaze or insufficient movement in primary gaze and up-gaze. The Percentage of subject eyes with acceptable lens fit will be reported.

  30 Minutes Post Insertion

• Percentage of Eyes With Acceptable Cosmetic Lens Fit

  Cosmetic lens fitting is assessed for each subject eye in the primary gaze position without a slit lamp. Cosmetic lens fit is a binary response and is reported as acceptable or unacceptable. The Percentage of subject eyes with acceptable cosmetic lens fitting is reported.

  30 Minutes Post Insertion

Study Arms (6)

Group Sequence A, B, C

ACTIVE COMPARATOR

Subjects will wear Test 1, Test 2, and Control contact lenses in order according to the randomization sequence assigned for approximately 30-60 minutes each, with a 5-minute wash-out period between lenses.

Device: Etafilcon A Design 1 (Test 1); Device: Etafilcon A Design 2 (Test 2); Device: Etafilcon A (Control)

Group Sequence B, C, A

ACTIVE COMPARATOR

Subjects will wear Test 1, Test 2, and Control contact lenses in order according to the randomization sequence assigned for approximately 30-60 minutes each, with a 5-minute wash-out period between lenses.

Device: Etafilcon A Design 1 (Test 1); Device: Etafilcon A Design 2 (Test 2); Device: Etafilcon A (Control)

Group Sequence C, A, B

ACTIVE COMPARATOR

Subjects will wear Test 1, Test 2, and Control contact lenses in order according to the randomization sequence assigned for approximately 30-60 minutes each, with a 5-minute wash-out period between lenses.

Device: Etafilcon A Design 1 (Test 1); Device: Etafilcon A Design 2 (Test 2); Device: Etafilcon A (Control)

Group Sequence C, B, A

ACTIVE COMPARATOR

Subjects will wear Test 1, Test 2, and Control contact lenses in order according to the randomization sequence assigned for approximately 30-60 minutes each, with a 5-minute wash-out period between lenses.

Device: Etafilcon A Design 1 (Test 1); Device: Etafilcon A Design 2 (Test 2); Device: Etafilcon A (Control)

Group Sequence A, C, B

ACTIVE COMPARATOR

Subjects will wear Test 1, Test 2, and Control contact lenses in order according to the randomization sequence assigned for approximately 30-60 minutes each, with a 5-minute wash-out period between lenses.

Device: Etafilcon A Design 1 (Test 1); Device: Etafilcon A Design 2 (Test 2); Device: Etafilcon A (Control)

Group Sequence B, A, C

ACTIVE COMPARATOR

Subjects will wear Test 1, Test 2, and Control contact lenses in order according to the randomization sequence assigned for approximately 30-60 minutes each, with a 5-minute wash-out period between lenses.

Device: Etafilcon A Design 1 (Test 1); Device: Etafilcon A Design 2 (Test 2); Device: Etafilcon A (Control)

Interventions

Etafilcon A Design 1 (Test 1) DEVICE

Group Sequence A, B, C; Group Sequence A, C, B; Group Sequence B, A, C; Group Sequence B, C, A; Group Sequence C, A, B; Group Sequence C, B, A

Etafilcon A Design 2 (Test 2) DEVICE

Group Sequence A, B, C; Group Sequence A, C, B; Group Sequence B, A, C; Group Sequence B, C, A; Group Sequence C, A, B; Group Sequence C, B, A

Etafilcon A (Control) DEVICE

Group Sequence A, B, C; Group Sequence A, C, B; Group Sequence B, A, C; Group Sequence B, C, A; Group Sequence C, A, B; Group Sequence C, B, A

Eligibility Criteria

• Age: 18 Years - 55 Years
• Sex: all
• Healthy Volunteers: Yes
• Age Groups: Adult (18-64)

You may qualify if:

• Subjects must be at least 18 years of age and no more than 55 years of age (inclusive).
• The subject's vertex corrected best spherical distance refraction must be in the range of -1.00 to -6.00 Diopters (D) in each eye.
• The subject's vertex corrected cylindrical component of distance refraction must be less than or equal to -1.50 Diopters of Cylinder (DC) in each eye.
• Subjects must have best corrected visual acuity of 20/25 (Snellen or equivalent) or better in each eye.
• Subjects must self-report as being Asian race.
• Subjects must self-report as having brown or black eyes.
• Subjects must be habitual lens wearer (clear or limbal ring cosmetic) . Habitual is defined as at least one (1) month of Contact Lens wear where the lenses were worn for a minimum of six (6) hours per day and a minimum of three (3) days per week.
• Subjects between 18 to 39 years old must be habitual limbal ring cosmetic lens wearers or must have tried limbal ring cosmetic lens within the past two years.
• Subjects must be cosmetic contact lens concept acceptors as determined by screening questionnaire.
• Subjects must possess a functional / usable pair of spectacles and bring them to the visit (only if applicable - to the investigator's discretion).
• Subjects must read, understand, and sign the Statement of Informed Consent.
• Subjects must appear able and willing to adhere to the instructions set forth in the clinical protocol.
• Subjects must be willing to have their eyes video recorded and photographed.

You may not qualify if:

• Working for any advertising agency, any company involved in public relations or marketing, market research; or any company that makes or sells contact lenses or glasses.
• Participated in any paid market research within the past 3 months.
• Pregnant or breast feeding a baby.
• Subjects with diabetes.
• Any ocular or systemic allergies or disease which might interfere with contact lens wear.
• Any systemic disease, or autoimmune disease, which might interfere with contact lens wear, at investigator's discretion.
• Using medications during and immediately preceding the study period that may interfere with current contact lens wear as determined by the investigators
• Any infectious diseases (e.g. hepatitis, tuberculosis) or a contagious immunosuppressive disease (e.g. HIV), by self-report.
• Any grade 3 or greater Biomicroscopy findings (this includes, corneal edema, corneal staining, corneal vascularization, conjunctival injection, tarsal abnormalities, bulbar injection) on the FDA classification scale.
• Any active ocular abnormalities/conditions that might interfere with contact lens wear (this includes, but not limited to, chalazia, recurrent styles, pterygium, infection etc.).
• Any corneal distortion, scar, or opacity affecting vision as noted by subjects or investigators during examination.
• History of any corneal surgery (e.g. radial keratotomy (RK), photorefractive keratectomy (PRK), laser-assisted in situ keratomileusis (LASIK)); confirmed with topography if necessary at the investigator's discretion.
• Habitual wearers of rigid gas permeable or orthokeratology lens within the past 3 months.
• Current habitual contact lens modality for extended wear or conventional wear (contact lenses with a replacement schedule of 3 months to \>1 year).
• Participation in any pharmaceutical, medical device, or contact lens related clinical research trial within 14 days prior to study enrollment. This excludes studies that do not require product treatment/intervention.

Sponsors & Collaborators

• Johnson & Johnson Vision Care, Inc.: lead

Study Sites (1)

Hong Kong Polytechnic University

Hong Hom, Kowloon, Hong Kong

Location

Results Point of Contact

• Title: Meredith Bishop, OD, MS, FAAO
• Organization: Johnson & Johnson Vision

MBishop4@its.jnj.com

904-443-1396

Publication Agreements

• PI is Sponsor Employee: No
• Restriction Type: GT60
• Restrictive Agreement: Yes

Study Design

• Study Type: interventional
• Phase: not applicable
• Allocation: RANDOMIZED
• Masking: NONE
• Purpose: TREATMENT
• Intervention Model: CROSSOVER
• Sponsor Type: INDUSTRY
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: May 11, 2016
• First Posted: June 15, 2016
• Study Start: April 24, 2016
• Primary Completion: May 22, 2016
• Study Completion: May 22, 2016
• Last Updated: July 11, 2017
• Results First Posted: June 9, 2017

Record last verified: 2017-06

Locations

HK (1)