Clinical Evaluation of Hydrogels vs Silicone Hydrogel Contact Lenses

NCT01966770 | Completed Results

• 1 other identifier: EX-MKTG-44
• Study Type: interventional
• Target: 20
• Locations: 1 country
• Sites: 1

Brief Summary

The aim of this fitting study is to evaluate the clinical performance of different hydrogel and silicone hydrogel contact lenses.

Conditions

Myopia

Outcome Measures

Primary Outcomes (35)

• Visual Acuity (VA) logMAR (Habitual Lenses)

  Assessment of high contrast distance visual acuity (VA). Collected at baseline with subject wearing habitual lens prior to dispense of study lens. (logMAR)

  Baseline

• Visual Acuity (VA) logMAR (Study Lenses)

  Assessment of high contrast distance visual acuity (VA). Collected at dispense of study lens. (logMAR)

  Dispense

• Comfort Contact Lens Insertion (Day 1 Study Lenses)

  Participant rating of comfort upon contact lens insertion. Collected after insertion at Day 1 for each lens . (0-100, 0=cannot be worn causes pain, 100=cannot be felt ever)

  Day 1 - Insertion

• Comfort Contact Lens 30 Minutes Wear (Day 1 Study Lenses)

  Participant rating of comfort after contact lens settling. Collected at 30 minutes wear for each lens. (0-100, 0=cannot be worn causes pain, 100=cannot be felt ever)

  Day 1 - 30 minutes

• Comfort Contact Lens Insertion (Day 2 Study Lenses)

  Participant rating of comfort upon contact lens insertion. Collected after insertion at Day 2 for each lens . (0-100, 0=cannot be worn causes pain, 100=cannot be felt ever

  Day 2 - Insertion

• Comfort Contact Lens 30 Minutes Wear (Day 2 Study Lenses)

  Participant rating of comfort upon contact lens insertion. Collected after 30 minutes of wear at Day 2 for each lens . (0-100, 0=cannot be be worn causes pain, 100=cannot be felt ever

  Day 2 - 30 minutes

• Comfort Preference Contact Lens Insertion (Day 1 Study Lenses - Pair 1)

  Participant rating of comfort preference upon contact lens insertion of pair 1. Collected at insertion for each lens. Percent of participants that strongly prefer lens or have No Preference. (forced choice preference for right or left eye; Strongly Prefer Left, Slightly Prefer Left, No Preference, Slightly Prefer Right, Strongly Prefer Right)

  Day 1 - Insertion

• Comfort Preference Contact Lens Insertion (Day 1 Study Lenses - Pair 2)

  Participant rating of comfort preference upon contact lens insertion of pair 2. Collected at insertion for each lens. Percent of participants that strongly prefer lens or have No Preference. (forced choice preference for right or left eye; Strongly Prefer Left, Slightly Prefer Left, No Preference, Slightly Prefer Right, Strongly Prefer Right)

  Day 1 Insertion

• Comfort Preference Contact Lens Insertion (Day 1 Study Lenses - Pair 3)

  Participant rating of comfort preference upon contact lens insertion of pair 3. Collected at insertion for each lens. Percent of participants that strongly prefer lens or have No Preference. (forced choice preference for right or left eye; Strongly Prefer Left, Slightly Prefer Left, No Preference, Slightly Prefer Right, Strongly Prefer Right)

  Day 1 - Insertion

• Comfort Preference Contact Lens 30 Minutes Wear (Day 1 Study Lenses - Pair 1)

  Participant rating of comfort preference upon contact lens settling of pair 1. Collected at 30 minutes post settling for each lens. Percent of participants that strongly prefer lens or have No Preference. (forced choice preference for right or left eye; Strongly Prefer Left, Slightly Prefer Left, No Preference, Slightly Prefer Right, Strongly Prefer Right)

  Day 1 - 30 minutes

• Comfort Preference Contact Lens 30 Minutes Wear (Day 1 Study Lenses - Pair 2)

  Participant rating of comfort preference upon contact lens settling of pair 2. Collected at 30 minutes post settling for each lens. Percent of participants that strongly prefer lens or have No Preference. (forced choice preference for right or left eye; Strongly Prefer Left, Slightly Prefer Left, No Preference, Slightly Prefer Right, Strongly Prefer Right)

  Day 1 - 30 minutes

• Comfort Preference Contact Lens 30 Minutes Wear (Day 1 Study Lenses - Pair 3)

  Participant rating of comfort preference upon contact lens settling of pair 3. Collected at 30 minutes post settling for each lens. Percent of participants that strongly prefer lens or have No Preference. (forced choice preference for right or left eye; Strongly Prefer Left, Slightly Prefer Left, No Preference, Slightly Prefer Right, Strongly Prefer Right)

  Day 1 - 30 minutes

• Comfort Preference Contact Lens Insertion (Day 2 Study Lenses - Pair 1)

  Participant rating of comfort preference upon contact lens insertion of pair 1. Collected at insertion for each lens. Percent of participants that strongly prefer lens or have No Preference. (forced choice preference for right or left eye; Strongly Prefer Left, Slightly Prefer Left, No Preference, Slightly Prefer Right, Strongly Prefer Right)

  Day 2 - Insertion

• Comfort Preference Contact Lens Insertion (Day 2 Study Lenses - Pair 2)

  Participant rating of comfort preference upon contact lens insertion of pair 2. Collected at insertion for each lens. Percent of participants that strongly prefer lens or have No Preference. (forced choice preference for right or left eye; Strongly Prefer Left, Slightly Prefer Left, No Preference, Slightly Prefer Right, Strongly Prefer Right)

  Day 2 - Insertion

• Comfort Preference Contact Lens Insertion (Day 2 Study Lenses - Pair 3)

  Participant rating of comfort preference upon contact lens insertion of pair 3. Collected at insertion for each lens. Percent of participants that strongly prefer lens or have No Preference. (forced choice preference for right or left eye; Strongly Prefer Left, Slightly Prefer Left, No Preference, Slightly Prefer Right, Strongly Prefer Right)

  Day 2 - Insertion

• Comfort Preference Contact Lens 30 Minutes Wear (Day 2 Study Lenses - Pair 1)

  Participant rating of comfort preference upon contact lens settling of pair 1. Collected at 30 minutes post settling for each lens. Percent of participants that strongly prefer lens or have No Preference. (forced choice preference for right or left eye; Strongly Prefer Left, Slightly Prefer Left, No Preference, Slightly Prefer Right, Strongly Prefer Right)

  Day 2 - 30 minutes

• Comfort Preference Contact Lens 30 Minutes Wear (Day 2 Study Lenses - Pair 2)

  Participant rating of comfort preference upon contact lens settling of pair 2. Collected at 30 minutes post settling for each lens. Percent of participants that strongly prefer lens or have No Preference. (forced choice preference for right or left eye; Strongly Prefer Left, Slightly prefer Left, No Preference, Slightly prefer Right, Strongly prefer Right)

  Day 2 - 30 minutes

• Comfort Preference Contact Lens 30 Minutes Wear (Day 2 Study Lenses - Pair 3)

  Participant rating of comfort preference upon contact lens settling of pair 3. Collected at 30 minutes post settling for each lens. Percent of participants that strongly prefer lens or have No Preference. (forced choice preference for right or left eye; Strongly Prefer Left, Slightly prefer Left, No Preference, Slightly prefer Right, Strongly prefer Right)

  Day 2 - 30 minutes

• Lens Fitting Characteristics, Centration (Habitual Lens)

  Assessment of habitual lens fitting characteristics for the percentage of lenses with optimal centration. Collected at baseline with subject wearing habitual lens prior to dispense of study lens. (Optimal Centration for Right and Left eyes; Optimum, Decentration Acceptable, Decentration unacceptable)

  Baseline

• Lens Fitting Characteristics, Tightness (Habitual Lens)

  Assessment of habitual lens fitting characteristics. Collected at baseline with subject wearing habitual lens prior to dispense of study lens. Digital push up test. (Continuous scale 0-100%, 0%=falls from cornea without lid support, 50%=optimum, 100%=no movement)

  Baseline

• Lens Fitting Characteristics, Upgaze Lag and Post-blink Movement (Habitual Lens)

  Assessment of habitual lens fitting characteristics. Collected at baseline with subject wearing habitual lens prior to dispense of study lens.(Upgaze Lag and Post-blink Movement in mm)

  Baseline

• Lens Fitting Characteristics, Centration (Day 1 Study Lenses)

  Assessment of lens fitting characteristics for the percentage of lenses with optimal centration. Collected at 30 minutes after lens settling of study lens. (Optimal Centration for Right and Left eyes; Optimum, Decentration Acceptable, Decentration unacceptable)

  Day 1 - 30 minutes

• Lens Fitting Characteristics, Push-up Tightness (Day 1 Study Lenses)

  Assessment of lens fitting characteristics. Collected at 30 minutes after lens settling of study lens. Digital push up test. (Continuous scale 0-100%, 0%=falls from cornea without lid support, 50%=optimum, 100%=no movement)

  Day 1 - 30 minutes

• Lens Fitting Characteristics, Upper Gaze Lag and Post-blink Movement (Day 1 - Study Lenses)

  Assessment of lens fitting characteristics. Collected at 30 minutes after lens settling of study lens. (Upgaze Lag and Post-blink Movement in mm)

  Day 1 - 30 minutes

• Lens Fitting Characteristics, Centration (Day 2 Study Lenses)

  Assessment of lens fitting characteristics for the percentage of lenses with optimal centration. Collected at 30 minutes after lens settling of study lens. (Optimal Centration for Right and Left eyes; Optimum, Decentration Acceptable, Decentration unacceptable)

  Day 2 - 30 minutes

• Lens Fitting Characteristics, Push-up Tightness (Day 2 Study Lenses)

  Assessment of lens fitting characteristics. Collected at 30 minutes after lens settling of study lens. Digital push up test. (Continuous scale 0-100%, 0%=falls from cornea without lid support, 50%=optimum, 100%=no movement)

  Day 2 - 30 minutes

• Lens Fitting Characteristics, Upper Gaze Lag and Post-blink Movement (Day 2 Study Lenses)

  Assessment of lens fitting characteristics. Collected at 30 minutes after lens settling of study lens.(Upgaze Lag and Post-blink Movement in mm)

  Day 2 - 30 minutes

• Investigator Fit Preference Contact Lens 30 Minutes Wear (Day 1 Study Lenses - Pair 1)

  Investigator rating of fit preference upon contact lens settling of pair 1. Collected at 30 minutes post settling for each lens. Percent of investigators that strongly prefer lens or have No Preference. (forced choice preference for right or left eye; Strong R, Slight R, No Pref, Slight L, Strong L)

  Day 1- 30 minutes

• Investigator Fit Preference Contact Lens 30 Minutes Wear (Day 1 Study Lenses - Pair 2)

  Investigator rating of fit preference upon contact lens settling of pair 2. Collected at 30 minutes post settling for each lens. Percent of investigators that strongly prefer lens or have No Preference. (forced choice preference for right or left eye; Strong R, Slight R, No Pref, Slight L, Strong L)

  Day 1- 30 minutes

• Investigator Fit Preference Contact Lens 30 Minutes Wear (Day 1 Study Lenses - Pair 3)

  Investigator rating of fit preference upon contact lens settling of pair 3. Collected at 30 minutes post settling for each lens. Percent of investigators that strongly prefer lens or have No Preference. (forced choice preference for right or left eye; Strong R, Slight R, No Pref, Slight L, Strong L)

  Day 1 - 30 minutes

• Investigator Fit Preference Contact Lens 30 Minutes Wear (Day 2 Study Lenses - Pair 1)

  Investigator rating of fit preference upon contact lens settling of pair 1. Collected at 30 minutes post settling for each lens. Percent of investigators that strongly prefer lens or have No Preference. (forced choice preference for right or left eye; Strong R, Slight R, No Pref, Slight L, Strong L)

  Day 2 - Insertion

• Investigator Fit Preference Contact Lens 30 Minutes Wear (Day 2 Study Lenses - Pair 2)

  Investigator rating of fit preference upon contact lens settling of pair 2. Collected at 30 minutes post settling for each lens. Percent of investigators that strongly prefer lens or have No Preference. (forced choice preference for right or left eye; Strong R, Slight R, No Pref, Slight L, Strong L)

  Day 2 - Insertion

• Investigator Preference Contact Lens 30 Minutes Wear (Day 2 Study Lenses - Pair 3)

  Investigator rating of fit preference upon contact lens settling of pair 3. Collected at 30 minutes post settling for each lens. Percent of investigators that strongly prefer lens or have No Preference. (forced choice preference for right or left eye; Strong R, Slight R, No Pref, Slight L, Strong L)

  Day 2 - Insertion

• Overall Ease of Lens Handling (Day 1 Study Lenses)

  Participant rating of overall lens handling regarding insertion and removal. Collected at post-removal for each lens on Day 1. (0-100, 0=very difficult, 100=very easy

  Day 1 - After Removal

• Overall Ease of Lens Handling (Day 2 Study Lenses)

  Participant rating of overall lens handling regarding insertion and removal. Collected at post-removal for each lens on Day 2. (0-100, 0=very difficult, 100=very easy

  Day 2 - After Removal

Study Arms (6)

Pair 1 (ocufilcon D / ocufilcon D)

ACTIVE COMPARATOR

Randomized to contra lateral lens pair 1 (ocufilcon D hydrogel / ocufilcon D hydrogel)

Device: Pair 1 (ocufilcon D / ocufilcon D)

Pair 2 (ocufilcon D / enfilcon A)

ACTIVE COMPARATOR

Randomized to contra lateral lens pair 2 (ocufilcon D hydrogel / enfilcon A silicone)

Device: Pair 2 (ocufilcon D / enfilcon A)

Pair 3 (ocufilcon D / comfilcon A)

ACTIVE COMPARATOR

Randomized to contra lateral lens pair 3 (ocufilcon D hydrogel / comfilcon A silicone)

Device: Pair 3 (ocufilcon D / comfilcon A)

Pair 4 (methafilcon A / methafilcon A)

ACTIVE COMPARATOR

Randomized to contra lateral lens pair 4 (methafilcon A hydrogel sphere / methafilcon A hydrogel asphere)

Device: Pair 4 (methafilcon A / methafilcon A)

Pair 5 (methafilcon A / comfilcon A)

ACTIVE COMPARATOR

Randomized to contra lateral lens pair 5 (methafilcon A hydrogel / comfilcon A silicone)

Device: Pair 5 (methafilcon A / comfilcon A)

Pair 6 (omafilcon A / comfilcon A)

ACTIVE COMPARATOR

Randomized to contra lateral lens pair 6 (omafilcon A hydrogel / comfilcon A silicone)

Device: Pair 6 (omafilcon A / comfilcon A)

Interventions

Pair 1 (ocufilcon D / ocufilcon D) DEVICE

Randomized to contra lateral lens pair 1 (ocufilcon D hydrogel / ocufilcon D hydrogel)

Pair 1 (ocufilcon D / ocufilcon D)

Pair 2 (ocufilcon D / enfilcon A) DEVICE

Randomized to contra lateral lens pair 2 (ocufilcon D hydrogel / enfilcon A silicone)

Pair 2 (ocufilcon D / enfilcon A)

Pair 3 (ocufilcon D / comfilcon A) DEVICE

Randomized to contra lateral lens pair 3 (ocufilcon D hydrogel / comfilcon A silicone)

Pair 3 (ocufilcon D / comfilcon A)

Pair 4 (methafilcon A / methafilcon A) DEVICE

Randomized to contra lateral lens pair 4 (methafilcon A hydrogel sphere / methafilcon A hydrogel asphere)

Pair 4 (methafilcon A / methafilcon A)

Pair 5 (methafilcon A / comfilcon A) DEVICE

Randomized to contra lateral lens pair 5 (methafilcon A hydrogel / comfilcon A silicone)

Pair 5 (methafilcon A / comfilcon A)

Pair 6 (omafilcon A / comfilcon A) DEVICE

Randomized to contra lateral lens pair 6 (omafilcon A hydrogel / comfilcon A silicone)

Pair 6 (omafilcon A / comfilcon A)

Eligibility Criteria

• Age: 18 Years - 40 Years
• Sex: all
• Healthy Volunteers: No
• Age Groups: Adult (18-64)

You may qualify if:

• Is between 18 and 40 years of age (inclusive)
• Has had a self-reported visual exam in the last two years
• Is an adapted soft contact lens wearer
• Has a cl spherical prescription between -1.00 and -6.00 (inclusive)
• Has a spectacle cylinder up to 0.75D (diopter) in each eye
• Is correctable to a visual acuity of 20/25 or better in both eyes
• Has clear corneas and no active ocular disease
• Has read, understood and signed the information consent letter
• Is willing to comply with the wear schedule
• Is willing to comply with the visit schedule

You may not qualify if:

• A person will be excluded from the study if he/she:
• Has never worn contact lenses before
• Currently wears rigid gas permeable contact lenses
• Has a history of not achieving comfortable contact lens wear (5 days per week; \> 8 hours/day)
• Has a contact lens prescription outside the range of -1.00 to -6.00D
• Has a spectacle cylinder ≥ 1.00D of cylinder in either eye
• Has best corrected spectacle distance vision worse than 20/25 in either eye
• Has any systemic or topical medications that will affect ocular health
• Has any ocular pathology or severe insufficiency of lacrimal secretion
• Has persistent, clinically significant corneal or conjunctival staining
• Has active neovascularization or any central corneal scars
• Is aphakic
• Is presbyopic
• Has undergone corneal refractive surgery
• Is participating in any other type of eye related conical or research study

Sponsors & Collaborators

• CooperVision, Inc.: lead

Study Sites (1)

University of California, Berkeley Clinical Research Center (UCB-CRC)

Berkeley, California, 94720-2020, United States

Location

MeSH Terms

Conditions

Myopia

Condition Hierarchy (Ancestors)

Refractive Errors; Eye Diseases

Results Point of Contact

• Title: Meng C. Lin O.D., PhD, FAAO
• Organization: Clinical Research Center-UC berkely

mlin@berkeley.edu

510-643-9252

Study Officials

• Meng Lin, OD PhD FAAO

  CRC-UC Berkeley

  PRINCIPAL INVESTIGATOR

Publication Agreements

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

Study Design

• Study Type: interventional
• Phase: not applicable
• Allocation: RANDOMIZED
• Masking: DOUBLE
• Who Masked: PARTICIPANT, INVESTIGATOR
• Purpose: TREATMENT
• Intervention Model: SINGLE GROUP
• Sponsor Type: INDUSTRY
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: October 15, 2013
• First Posted: October 22, 2013
• Study Start: October 1, 2013
• Primary Completion: November 1, 2013
• Study Completion: November 1, 2013
• Last Updated: July 30, 2020
• Results First Posted: February 27, 2015

Record last verified: 2020-07

Locations

US (1)