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A Bilateral Dispensing Clinical Trial of an Sapphire Lens Against Senofilcon A Toric for Astigmatism Lens

Primary Purpose

Astigmatism

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Sapphire contact lenses
senofilcon A contact lenses
Sponsored by
Coopervision, Inc.
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Astigmatism

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • A person is eligible for inclusion in the study if they:

    1. Are at least 18 years of age and have full legal capacity to volunteer;
    2. Have read and signed an information consent letter;
    3. Are willing and able to follow instructions and maintain the appointment schedule;
    4. Are an adapted soft contact lens wearer;
    5. Require spectacle lens powers in both eyes;

      1. Sphere: between -1.75 to -6.00 diopters and
      2. Astigmatism: between -1.00 to -2.25 and
      3. Axis: 180 ± 20 degrees
    6. Are willing to wear contact lenses in both eyes;
    7. Have manifest refraction visual acuities (VA) equal to or better than logMAR (log of the minimum angle of resolution) equivalent of 20/25 in each eye;
    8. To be eligible for lens dispensing, the subject must have VA of logMAR equivalent of 20/30 or better in each eye with the study lenses and the investigator must judge the fit including toric orientation as acceptable.

Exclusion Criteria:

  • A person will be excluded from the study if they:

    1. Are participating in any concurrent clinical or research study;
    2. Have any known active* ocular disease and/or infection;
    3. Have a systemic condition that in the opinion of the investigator may affect a study outcome variable;
    4. Are using any systemic or topical medications that in the opinion of the investigator may affect a study outcome variable;
    5. Have known sensitivity to the diagnostic pharmaceuticals to be used in the study;
    6. Are pregnant, lactating or planning a pregnancy at the time of enrolment (by verbal confirmation at the screening visit);
    7. Are aphakic;
    8. Have undergone refractive error surgery;

Sites / Locations

  • Family Eye Care Center

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Sapphire contact lenses

senofilcon A

Arm Description

Each subject randomized to wear either the Investigational lenses (test) or senofilcon A contact lenses (control) as a matched pair and cross over to the second matched pair.

Each subject randomized to wear either the Investigational lenses (test) or senofilcon A contact lenses (control) as a matched pair and cross over to the second matched pair.

Outcomes

Primary Outcome Measures

Subjective Ratings for Comfort
Scale 0-100; (0=Cannot be worn; 100=Cannot be felt ever)
Subjective Ratings for Comfort
Scale 0-100; (0=Cannot be worn; 100=Cannot be felt ever)
Subjective Ratings for Comfort Preference
Subjective Ratings for Comfort Preference: Sapphire lens, senofilcon A lens, No preference
Subjective Ratings for Comfort Preference
Subjective Ratings for Comfort Preference: Sapphire lens, senofilcon A lens, No preference
Subjective Assessment of Visual Quality
Subjective assessment of visual quality assessed on a Scale: 0-100 (0=Extremely poor vision all of the time; Cannot function; 100=Excellent vision all of the time)
Subjective Assessment of Visual Quality
Subjective assessment of visual quality assessed on a Scale: 0-100 (0=Extremely poor vision all of the time; Cannot function; 100=Excellent vision all of the time)
Subjective Assessment of Overall Satisfaction
Subjective assessment of overall satisfaction on a Scale: 0-100: (0=Extremely dissatisfied; 100=Extremely satisfied)
Subjective Assessment of Overall Satisfaction
Subjective assessment of overall satisfaction on a Scale: 0-100: (0=Extremely dissatisfied; 100=Extremely satisfied)
Subjective Overall Preference
Subjective Overall Preference: Sapphire lens, senofilcon A lens, No preference
Subjective Overall Preference
Subjective Overall Preference: Sapphire lens, senofilcon A lens, No preference

Secondary Outcome Measures

Full Information

First Posted
September 4, 2015
Last Updated
September 22, 2020
Sponsor
Coopervision, Inc.
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1. Study Identification

Unique Protocol Identification Number
NCT02555098
Brief Title
A Bilateral Dispensing Clinical Trial of an Sapphire Lens Against Senofilcon A Toric for Astigmatism Lens
Official Title
A Bilateral Dispensing Clinical Trial of Sapphire Lens Against Senofilcon A Toric for Astigmatism Lens Over 2 Weeks
Study Type
Interventional

2. Study Status

Record Verification Date
September 2020
Overall Recruitment Status
Completed
Study Start Date
September 2015 (undefined)
Primary Completion Date
February 2016 (Actual)
Study Completion Date
April 2016 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Coopervision, Inc.

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
This study was conducted to evaluate the clinical performance of an investigational silicone-hydrogel lens against Senofilcon A toric lens. The study results were not used for design validation of the investigational product.
Detailed Description
This will be a randomized, bilateral, 2-week cross-over, double-masked, dispensing study comparing the investigational test lens against the Senofilcon A Toric for Astigmatism control lens.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Astigmatism

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Crossover Assignment
Masking
ParticipantInvestigator
Allocation
Randomized
Enrollment
23 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Sapphire contact lenses
Arm Type
Experimental
Arm Description
Each subject randomized to wear either the Investigational lenses (test) or senofilcon A contact lenses (control) as a matched pair and cross over to the second matched pair.
Arm Title
senofilcon A
Arm Type
Active Comparator
Arm Description
Each subject randomized to wear either the Investigational lenses (test) or senofilcon A contact lenses (control) as a matched pair and cross over to the second matched pair.
Intervention Type
Device
Intervention Name(s)
Sapphire contact lenses
Intervention Description
Each subject randomized to wear either the test or control contact lenses as a matched pair and cross over to the second matched pair
Intervention Type
Device
Intervention Name(s)
senofilcon A contact lenses
Intervention Description
Each subject randomized to wear either the test or control contact lenses as a matched pair and cross over to the second matched pair
Primary Outcome Measure Information:
Title
Subjective Ratings for Comfort
Description
Scale 0-100; (0=Cannot be worn; 100=Cannot be felt ever)
Time Frame
Baseline (10 minutes post lens settling)
Title
Subjective Ratings for Comfort
Description
Scale 0-100; (0=Cannot be worn; 100=Cannot be felt ever)
Time Frame
2 weeks
Title
Subjective Ratings for Comfort Preference
Description
Subjective Ratings for Comfort Preference: Sapphire lens, senofilcon A lens, No preference
Time Frame
Baseline (10 minutes post lens settling)
Title
Subjective Ratings for Comfort Preference
Description
Subjective Ratings for Comfort Preference: Sapphire lens, senofilcon A lens, No preference
Time Frame
2 weeks
Title
Subjective Assessment of Visual Quality
Description
Subjective assessment of visual quality assessed on a Scale: 0-100 (0=Extremely poor vision all of the time; Cannot function; 100=Excellent vision all of the time)
Time Frame
Baseline (10 minutes post lens settling)
Title
Subjective Assessment of Visual Quality
Description
Subjective assessment of visual quality assessed on a Scale: 0-100 (0=Extremely poor vision all of the time; Cannot function; 100=Excellent vision all of the time)
Time Frame
2 weeks
Title
Subjective Assessment of Overall Satisfaction
Description
Subjective assessment of overall satisfaction on a Scale: 0-100: (0=Extremely dissatisfied; 100=Extremely satisfied)
Time Frame
Baseline (10 minutes post lens settling)
Title
Subjective Assessment of Overall Satisfaction
Description
Subjective assessment of overall satisfaction on a Scale: 0-100: (0=Extremely dissatisfied; 100=Extremely satisfied)
Time Frame
2 weeks
Title
Subjective Overall Preference
Description
Subjective Overall Preference: Sapphire lens, senofilcon A lens, No preference
Time Frame
Baseline (10 minutes post lens settling)
Title
Subjective Overall Preference
Description
Subjective Overall Preference: Sapphire lens, senofilcon A lens, No preference
Time Frame
2 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: A person is eligible for inclusion in the study if they: Are at least 18 years of age and have full legal capacity to volunteer; Have read and signed an information consent letter; Are willing and able to follow instructions and maintain the appointment schedule; Are an adapted soft contact lens wearer; Require spectacle lens powers in both eyes; Sphere: between -1.75 to -6.00 diopters and Astigmatism: between -1.00 to -2.25 and Axis: 180 ± 20 degrees Are willing to wear contact lenses in both eyes; Have manifest refraction visual acuities (VA) equal to or better than logMAR (log of the minimum angle of resolution) equivalent of 20/25 in each eye; To be eligible for lens dispensing, the subject must have VA of logMAR equivalent of 20/30 or better in each eye with the study lenses and the investigator must judge the fit including toric orientation as acceptable. Exclusion Criteria: A person will be excluded from the study if they: Are participating in any concurrent clinical or research study; Have any known active* ocular disease and/or infection; Have a systemic condition that in the opinion of the investigator may affect a study outcome variable; Are using any systemic or topical medications that in the opinion of the investigator may affect a study outcome variable; Have known sensitivity to the diagnostic pharmaceuticals to be used in the study; Are pregnant, lactating or planning a pregnancy at the time of enrolment (by verbal confirmation at the screening visit); Are aphakic; Have undergone refractive error surgery;
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Michel Guillon
Organizational Affiliation
Ocular Technology Group
Official's Role
Principal Investigator
Facility Information:
Facility Name
Family Eye Care Center
City
Campbell
State/Province
California
ZIP/Postal Code
95008
Country
United States

12. IPD Sharing Statement

Learn more about this trial

A Bilateral Dispensing Clinical Trial of an Sapphire Lens Against Senofilcon A Toric for Astigmatism Lens

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