Evaluating Soft Contact Lens Prototypes for Myopia Control

Visual Acuity Clinical Trial

Official title:

Evaluating Soft Contact Lens Prototypes for Myopia Control

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT03408444
• Other study ID #: CR-5959
• Status: Completed
• Start date: December 27, 2017
• Est. completion date: May 25, 2019

Study information

• Verified date: May 2022
• Source: Johnson & Johnson Vision Care, Inc.
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This is a multi-site, prospective, randomized, controlled, double-masked, four-arm-parallel-group, dispensing study. Each subject will be bilaterally fitted with one of four types of test articles and wear contact lenses of the assigned lens type during the entire course of the study. Test articles will be worn a minimum 8 hours per day and 5 days per week (subjects will be encouraged to wear study contact lenses 10 hours or more per day and 7 days per week) in a daily disposable modality for a minimum of 6 months and up to 1 year for a total of 7 scheduled visits.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 240
• Est. completion date: May 25, 2019
• Est. primary completion date: May 25, 2019
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 7 Years to 12 Years

Eligibility

Inclusion Criteria:

• Potential subjects must satisfy all of the following criteria to be enrolled in the study:

1. The subject must read (or be read to), understand, and sign the Statement of Information and Assent and receive a fully executed copy of the form.

2. The subject's parent(s) or legal guardian(s) must read, understand and sign the Statement of Informed Consent and receive a fully executed copy of the form.

3. Appear able and willing to adhere to the instructions set forth in this clinical protocol.

4. Between 7 and 12 years of age (inclusive).

5. Have normal eyes (i.e., no ocular medications or infections of any type).

6. Distance subjective best-sphere refraction must be between -0.75D and -4.50D (inclusive) in each eye.

7. Cylindrical refraction must be 1.00D or less in each eye, by subjective sphero-cylindrical refraction.

8. Have sphero-cylindrical best-corrected visual acuity of 20/25 (ie, 0.8 in decimal convention or 0.10 logMAR) or better in each eye.

9. Cycloplegic objective sphero-cylindrical refraction (by auto refraction) must be between -0.75D and -4.50D in sphere and is 1.00D or less in cylinder in each eye (based on the average of 5 repeated sphero-cylindrical refraction measures).

10. The difference in spherical equivalent power between the two eyes must be less than 1.50D (based on the average of 5 repeated sphero-cylindrical refraction measures).

Exclusion Criteria:

• Potential subjects who meet any of the following criteria will be excluded from participating in the study:

1. Currently pregnant or lactating.

2. Any systemic allergies, infectious disease (e.g., hepatitis, tuberculosis), autoimmune disease (e.g., rheumatoid arthritis), or other systemic diseases (e.g., diabetes), by the parent or legal guardian's report, which are known to interfere with contact lens wear and/or participation in the study.

3. Use of systemic medications (e.g., chronic steroid use) that are known to interfere with contact lens wear.

4. Any current use of ocular topical medication.

5. Any previous or planned ocular or intraocular surgery, including refractive surgery.

6. Participation in any contact lens or lens care product clinical trial within 30 days prior to study enrollment.

7. Participation in any prior myopia control clinical study in the test group.

8. Current or recent (within 30 days from enrollment) rigid lens wearers.

9. History of orthokeratology treatment or use of other ophthalmic devices (e.g., bifocal, multifocal contact or spectacle lenses) or drugs (e.g., atropine or pirenzepine) for the purpose of controlling myopia progression.

10. Any known hypersensitivity or allergic reaction to EyeCept® (or sponsor approved equivalent) Rewetting Drop Solution.

11. Relatives of employee of investigational clinic (e.g., Investigator, Coordinator, Technician).

12. Any ocular allergies, infections or other ocular abnormalities that are known to interfere with contact lens wear and/or participation in the study. This may include, but not be limited to, aphakia, uveitis, ocular hypertension, glaucoma, severe keratoconjunctivitis sicca, history of recurrent corneal erosions, keratoconus, keratoconus suspect, pellucid marginal degeneration, entropion, ectropion, extrusions, chalazia, and recurrent styes.

13. Grade 3 or greater palpebral conjunctival observations or any other grade 2 or greater slit lamp findings (e.g., edema, corneal neovascularization, corneal staining, conjunctival injection) on the ISO 11980 classification scale.

14. Any previous history or signs of a contact lens-related corneal inflammatory event (e.g., past peripheral ulcer or round peripheral scar), or any other ocular abnormality that may contraindicate contact lens wear.

15. Any central corneal scar

16. Any corneal distortion resulting from ocular diseases or previous hard or rigid gas permeable contact lens wear.

17. Binocular vision abnormality, intermittent strabismus or strabismus.

Related Conditions & MeSH terms

• Myopia
• Visual Acuity

Intervention

Device:
• EMO-114
Subjects between the ages of 7 and 12 years old will be bilaterally fitted with one of the four types of test articles and wear lenses of the assigned lens type during the entire course of the study.
• EMO-116
Subjects between the ages of 7 and 12 years old will be bilaterally fitted with one of the four types of test articles and wear lenses of the assigned lens type during the entire course of the study.
• EMO-118
Subjects between the ages of 7 and 12 years old will be bilaterally fitted with one of the four types of test articles and wear lenses of the assigned lens type during the entire course of the study.
• EMO-117
Subjects between the ages of 7 and 12 years old will be bilaterally fitted with one of the four types of test articles and wear lenses of the assigned lens type during the entire course of the study.

Locations

Country	Name	City	State
China	Fudan University Shanghai EENT Hospital	Shanghai

Sponsors (1)

Lead Sponsor	Collaborator
Johnson & Johnson Vision Care, Inc.

Country where clinical trial is conducted

China, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Axial Length	Axial length (in the unit of mm) was measured by a commercially available device based on the interferometry technique.	6-month follow-up
Primary	Spherical Equivalent of Cycloplegic Autorefraction (SECAR)	SECAR (in the unit of D) was computed from the spherocylindrical refraction measured by a commercially available autorefractor.	6-month follow-up