- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01494545
Performance Evaluation of DAILIES® TOTAL1™ in First Time Contact Lens Wearers
July 12, 2013 updated by: Alcon Research
The purpose of this study was to evaluate the performance of DAILIES® TOTAL1™ in first time contact lens wearers.
Study Overview
Study Type
Interventional
Enrollment (Actual)
102
Phase
- Not Applicable
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years to 44 years (Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Sign Informed Consent.
- No previous contact lens experience or attempt to try contact lenses (neophyte).
- Willing to wear study lenses for at least 8 hours a day for at least 5 days a week.
- Use spectacle lenses for vision correction.
- Other protocol-defined inclusion criteria may apply.
Exclusion Criteria:
- 45 years or older.
- Prior wear experience with rigid or soft contact lenses.
- Systemic or ocular disease or disorder that would negatively affect the conduct or outcome of the study.
- History of ocular surgery/trauma within the last six months.
- Pregnant or nursing women.
- Participation in any other ophthalmic drug or device clinical trial within 30 days of enrollment.
- Other protocol-defined exclusion criteria may apply.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Delefilcon A
Delefilcon A contact lenses worn in both eyes on a daily wear, daily disposable basis for two weeks.
A new pair was inserted each day.
|
Silicone hydrogel contact lens CE-marked for single use, daily disposable wear
Other Names:
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Initial Comfort
Time Frame: Day 1
|
Initial comfort was rated by the participant and recorded on a questionnaire at time of lens dispense.
Initial comfort was rated on a 10-point scale (1=poor to 10=excellent) as a single assessment for both eyes.
|
Day 1
|
|
Comfort at Insertion by Visit
Time Frame: Day 7, Day 14
|
Comfort at insertion was rated by the participant and recorded on a questionnaire as a single, retrospective evaluation of the previous week of lens wear.
Comfort at insertion was rated on a 10-point scale (1=poor to 10=excellent) as a single assessment for both eyes.
|
Day 7, Day 14
|
|
Comfort During the Day by Visit
Time Frame: Day 7, Day 14
|
Comfort during the day was rated by the participant and recorded on a questionnaire as a single, retrospective evaluation of the previous week of lens wear.
Comfort during the day was rated on a 10-point scale (1=poor to 10=excellent) as a single assessment for both eyes.
|
Day 7, Day 14
|
|
Comfort at End of Day by Visit
Time Frame: Day 7, Day 14
|
Comfort at end of day was rated by the participant and recorded on a questionnaire as a single, retrospective evaluation of the previous week of lens wear.
Comfort at end of day was rated on a 10-point scale (1=poor to 10=excellent) as a single assessment for both eyes.
|
Day 7, Day 14
|
|
Overall Comfort by Visit
Time Frame: Day 7, Day 14
|
Overall comfort was rated by the participant and recorded on a questionnaire as a single, retrospective evaluation of the previous week of lens wear.
Overall comfort was rated on a 10-point scale (1=poor to 10=excellent) as a single assessment for both eyes.
|
Day 7, Day 14
|
|
Initial Quality of Vision
Time Frame: Day 1
|
Initial quality of vision was rated by the participant and recorded on a questionnaire at time of lens dispense.
Initial quality of vision was rated on a 10-point scale (1=poor to 10=excellent) as a single assessment for both eyes.
|
Day 1
|
|
Quality of Vision at Insertion by Visit
Time Frame: Day 7, Day 14
|
Quality of vision at insertion was rated by the participant and recorded on a questionnaire as a single, retrospective evaluation of the previous week of lens wear.
Quality of vision at insertion was rated on a 10-point scale (1=poor to 10=excellent) as a single assessment for both eyes.
|
Day 7, Day 14
|
|
Quality of Vision During the Day by Visit
Time Frame: Day 7, Day 14
|
Quality of vision during the day was rated by the participant and recorded on a questionnaire as a single, retrospective evaluation of the previous week of lens wear.
Quality of vision during the day was rated on a 10-point scale (1=poor to 10=excellent) as a single assessment for both eyes.
|
Day 7, Day 14
|
|
Quality of Vision at End of Day by Visit
Time Frame: Day 7, Day 14
|
Quality of vision at end of day was rated by the participant and recorded on a questionnaire as a single, retrospective evaluation of the previous week of lens wear.
Quality of vision at end of day was rated on a 10-point scale (1=poor to 10=excellent) as a single assessment for both eyes.
|
Day 7, Day 14
|
|
Overall Quality of Vision by Visit
Time Frame: Day 7, Day 14
|
Overall quality of vision was rated by the participant and recorded on a questionnaire as a single, retrospective evaluation of the previous week of lens wear.
Overall quality of vision was rated on a 10-point scale (1=poor to 10=excellent) as a single assessment for both eyes.
|
Day 7, Day 14
|
|
Average Comfortable Daily Wear Time by Visit
Time Frame: Day 7, Day 14
|
Average comfortable daily wear time was reported by the participant as a single, retrospective evaluation of the previous week of wear.
|
Day 7, Day 14
|
|
Likert Statement: These Contact Lenses Were so Comfortable That I Don't Feel Anything.
Time Frame: Day 14
|
The participant indicated agreement/disagreement with the statement by using a 4-point scale: 2=Strongly Agree; 1=Agree; -1=Disagree; -2=Strongly Disagree.
A single assessment was made for both eyes.
|
Day 14
|
|
Likert Statement: These Contact Lenses Were so Comfortable That I Barely Felt Anything.
Time Frame: Day 14
|
The participant indicated agreement/disagreement with the statement by using a 4-point scale: 2=Strongly Agree; 1=Agree; -1=Disagree; -2=Strongly Disagree.
A single assessment was made for both eyes.
|
Day 14
|
|
Likert Statement: These Contact Lenses Felt so Comfortable That I Forgot I Was Wearing Them.
Time Frame: Day 14
|
The participant indicated agreement/disagreement with the statement by using a 4-point scale: 2=Strongly Agree; 1=Agree; -1=Disagree; -2=Strongly Disagree.
A single assessment was made for both eyes.
|
Day 14
|
|
Likert Statement: These Contact Lenses Are Perfect for When I Choose Not to Wear my Eye Glasses.
Time Frame: Day 14
|
The participant indicated agreement/disagreement with the statement by using a 4-point scale: 2=Strongly Agree; 1=Agree; -1=Disagree; -2=Strongly Disagree.
A single assessment was made for both eyes.
|
Day 14
|
|
Likert Statement: I Liked These Contact Lenses so Much That I Will Recommend Them to my Friends.
Time Frame: Day 14
|
The participant indicated agreement/disagreement with the statement by using a 4-point scale: 22=Strongly Agree; 1=Agree; -1=Disagree; -2=Strongly Disagree.
A single assessment was made for both eyes.
|
Day 14
|
|
Likert Statement: Overall, my Vision is Better With These Contact Lenses Compared to my Eye Glasses.
Time Frame: Day 14
|
The participant indicated agreement/disagreement with the statement by using a 4-point scale: 2=Strongly Agree; 1=Agree; -1=Disagree; -2=Strongly Disagree.
A single assessment was made for both eyes.
|
Day 14
|
|
Likert Statement: At the End of the Day my Vision is Better With These Contacts Lenses Compared to my Eye Glasses.
Time Frame: Day 14
|
The participant indicated agreement/disagreement with the statement by using a 4-point scale: 2=strongly agree; 1=agree; -1=disagree; -2=strongly disagree.
A single assessment was made for both eyes.
|
Day 14
|
|
Likert Statement: My Peripheral Vision is Better With These Contact Lenses Than With my Eye Glasses.
Time Frame: Day 14
|
The participant indicated agreement/disagreement with the statement by using a 4-point scale: 2=Strongly Agree; 1=Agree; -1=Disagree; -2=Strongly Disagree.
A single assessment was made for both eyes.
|
Day 14
|
|
Likert Statement: Compared to my Eye Glasses, my Vision With These Contact Lenses is:
Time Frame: Day 14
|
The participant indicated overall satisfaction/dissatisfaction with the contact lenses using a 5-point scale: 2=Much Better; 1=A Little Better; 0=Same; -1=A Little Worse; -2=Much Worse.
A single assessment was made for both eyes.
|
Day 14
|
|
Likert Statement: I am Interested in Purchasing These Contact Lenses.
Time Frame: Day 14
|
The participant indicated purchase intent using a 4-point scale: 2=Very Interested; 1=Interested; -1=Not Interested; -2=Very Disinterested.
A single assessment was made for both eyes.
|
Day 14
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Lens Surface Characteristics: Dry Areas/Non-wetting
Time Frame: Day 1
|
The investigator assessed the surface of the contact lens while the lens was on the participant's eye for dry areas/non-wetting: 0=None; 1=Very Slight; 2-Slight; 3=Moderate; 4=Severe.
Assessments were made individually (by eye) and binocularly (both eyes together).
|
Day 1
|
|
Lens Surface Characteristics: Dry Areas/Non-Wetting
Time Frame: Day 7
|
The investigator assessed the surface of the contact lens while the lens was on the participant's eye for dry areas/non-wetting: 0=None; 1=Very Slight; 2-Slight; 3=Moderate; 4=Severe.
Assessments were made individually (by eye) and binocularly (both eyes together).
|
Day 7
|
|
Lens Surface Characteristics: Dry Areas/Non-Wetting
Time Frame: Day 14
|
The investigator assessed the surface of the contact lens while the lens was on the participant's eye for dry areas/non-wetting: 0=None; 1=Very Slight; 2-Slight; 3=Moderate; 4=Severe.
Assessments were made individually (by eye) and binocularly (both eyes together).
|
Day 14
|
|
Duration of Overall Training Time
Time Frame: Day 1
|
The investigator recorded the time it took for the patient to insert both lenses and remove both lenses, not including instructions.
|
Day 1
|
|
Investigator's Satisfaction With Lens Fit by Visit
Time Frame: Day 1, Day 7, Day 14
|
The investigator considered the factors that relate to a well-fitted contact lens, including good centration, adequate movement, and complete corneal coverage, and rated his/her satisfaction with the contact lens fit on 10-point scale, with 1 being not at all satisfied and 10 being very satisfied.
|
Day 1, Day 7, Day 14
|
|
Investigator's Overall Impression of Surface Wettability by Visit
Time Frame: Day 1, Day 7, Day 14
|
The investigator rated his/her overall impression of the surface wettability of the contact lens on a 10-point scale (1=poor to 10=excellent).
|
Day 1, Day 7, Day 14
|
|
Investigator's Rating of Ease of Fit
Time Frame: Day 14
|
The investigator indicated agreement/disagreement with the statement, "The study lenses were easy to fit for this subject," by using a 4-point scale: 1=Strongly Agree; 2=Agree; 3=Disagree; 4=Strongly Disagree.
|
Day 14
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
December 1, 2011
Primary Completion (Actual)
April 1, 2012
Study Completion (Actual)
April 1, 2012
Study Registration Dates
First Submitted
December 15, 2011
First Submitted That Met QC Criteria
December 15, 2011
First Posted (Estimate)
December 19, 2011
Study Record Updates
Last Update Posted (Estimate)
July 19, 2013
Last Update Submitted That Met QC Criteria
July 12, 2013
Last Verified
July 1, 2013
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- P-347-C-016
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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