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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01055132
Other study ID # CR-1476AG
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date January 2010
Est. completion date February 2010

Study information

Verified date May 2015
Source Johnson & Johnson Vision Care, Inc.
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this study is to determine the relative performance of a new daily disposable toric soft contact lens against a daily disposable toric contact lens currently available in market, specifically with regards to the comfort and vision with the lens.


Recruitment information / eligibility

Status Completed
Enrollment 70
Est. completion date February 2010
Est. primary completion date February 2010
Accepts healthy volunteers No
Gender All
Age group 18 Years to 40 Years
Eligibility Inclusion Criteria:

- The subject must be between 18 and 40 years old.

- The subject must have normal eyes.

- The subject must appear able and willing to adhere to the instructions set forth in this clinical protocol.

- The subject must read and sign the STATEMENT OF INFORMED CONSENT and be provided a copy of the form.

- The subject must have a subjective distance spectacle prescription in the range of -1.75 to -5.00D in each eye.

- The subject must manifest -1.25 to -2.00 D of refractive astigmatism in each eye.

- The subject's refractive cylinder axis must be 180 degrees plus or minus 30 degrees in each eye.

- The subject must be an adapted wearer of soft toric contact lenses in both eyes.

- The subject's best visual acuity (BVA) must be better than or equal to 20/25 in each eye.

- Subjects must already possess a wearable pair of spectacles.

Exclusion Criteria:

- Ocular or systemic allergies or disease that may interfere with contact lens wear.

- Systemic disease or autoimmune disease or use of medication, which may interfere with contact lens wear.

- Clinically significant (grade 3 or 4) corneal edema, corneal vascularization, corneal staining or any other abnormality of the cornea, which may contraindicate contact lens wear.

- Clinically significant (grade 3 or 4) tarsal abnormalities that might interfere with contact lens wear.

- Any ocular infection.

- Any corneal distortion resulting from previous hard or rigid gas permeable contact lens wear.

- Pregnancy or lactation

- Any infectious disease (e.g., hepatitis, tuberculosis) or an immunosuppressive disease (e.g., HIV).

- Diabetes

- Strabismus

Study Design


Related Conditions & MeSH terms


Intervention

Device:
Etafilcon A toric contact lens
contact lens to correct astigmatism
Nelfilcon A toric contact lens
contact lens to correct astigmatism

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Johnson & Johnson Vision Care, Inc.

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Monocular Visual Acuity on LogMAR Scale Distance (4 meter) high contrast standard resolution (ETDRS) acuity was measured twice for each eye. Visual acuity describes the acuteness or sharpness of vision; the ability to perceive small details. Visual acuity is a measure of spacial resolution of the visual processing system; it's tested by requiring the person being tested to identify characters (like letters and numbers)on a chart from a set distance. LogMAR charts are used to assess visual acuity for research studies. LogMAR means Minimum Angle of Resolution. This has lead to the assertion that research is done using a logarithmic progression in size of letters on a test chart gives the most accurate visual acuity measurement. The reason for this is, unlike other charts, LogMAR chart has equal gradation between the letters on the line and the space between the lines. And, there is a fixed number of letters per line. After 5 to 9 days of lens wear
Primary Binocular Visual Acuity on LogMAR Scale Distance (4 meter) high contrast standard resolution (ETDRS) acuity was measured twice binocularly. Distance (4 meter) high contrast standard resolution (ETDRS) acuity was measured twice for each eye. Visual acuity describes the acuteness or sharpness of vision; the ability to perceive small details. Visual acuity is a measure of spacial resolution of the visual processing system; it's tested by requiring the person being tested to identify characters (like letters and numbers)on a chart from a set distance. LogMAR charts are used to assess visual acuity for research studies. LogMAR means Minimum Angle of Resolution. This has lead to the assertion that research is done using a logarithmic progression in size of letters on a test chart gives the most accurate visual acuity measurement. The reason for this is, unlike other charts, LogMAR chart has equal gradation between the letters on the line and the space between the lines. And, there is a fixed number of letters per line. After 5 to 9 days of lens wear
Primary Subject Reported Overall Lens Comfort Using the Contact Lens User Evaluation (CLUE)TM Questionnaire The Contact Lens User Evaluation(CLUE)TM questionnaire 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 +/-3*SD). After 5 to 9 days of lens wear
Primary Subject Reported Overall Quality of Vision Using the Contact Lens User Evaluation(CLUE)TM Questionnaire. The Contact Lens User Evaluation(CLUE)TM questionnaire 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 +/-3*SD). After 5 to 9 days of lens wear
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