Clinical Trials Logo

Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT06064617
Other study ID # 2023H0080
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date November 1, 2023
Est. completion date December 31, 2024

Study information

Verified date October 2023
Source Ohio State University
Contact Ann M Morrison, OD, PhD
Phone 614-247-0010
Email morrison.421@osu.edu
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Soft multifocal contact lenses are used for a variety of reasons in patient care. Multifocal contact lenses are most often used to correct presbyopic vision by providing a range of clear vision at both distance and near. Multifocal contact lenses correct vision at different distances by introducing a power gradient over the eye. They are designed using center near or center distance designs. For center near designs, the near addition is place in the center of the lens, and the power becomes more negative in the periphery. Conversely, for center distance designs, the distance prescription is placed in the center, and the power of the lens becomes more positive in the periphery in order to provide the near addition. Center near and distance designs have varying advantages and disadvantages for presbyopic vision correction, so a fitter may choose a specific design based on a patient's individual visual needs. Generally, it is thought that center near designs provide the most accommodative relief and superior near vision because the near addition is centered in the pupil and able to allow maximum near correction, even with miotic pupil size changes associated with accommodation. Plus lenses, or add powers, in spectacles are often used in the management of accommodative and binocular vision disorders. An add power, or plus lens, relieves accommodative demand. There is conflicting evidence on whether the add power in soft multifocal contact lenses can be used to manage accommodative and binocular vision disorders. Some case reports demonstrate benefits of multifocal contact lenses in accommodative insufficiency and convergence excess but the evidence is not clear and many previous studies utilize lenses that are not readily used anymore. Studies show that soft multifocal contact lenses alter accommodation in participants who wear lenses, but most studies use enter-distance lens designs, which is the most commonly used lens for myopia management. Most studies that have evaluated accommodative ability and function while wearing soft multifocal contact lenses have examined center distance lenses. Because center distance lenses are used for myopia management, the interest has been to determine if children maintain normal accommodative function while wearing the lenses. Accommodative function while wearing center near lenses has likely not been studied often because these lens designs are used most in presbyopic populations who have no or waning accommodative ability and are using the lenses, specifically, to account for that accommodative inability.-Knowing how spectacle lenses with add powers effectively treat some binocular vision and accommodative disorders and understanding how center near multifocal contact lenses correct presbyopic vision, it is reasonable to hypothesize that center near multifocal contact lenses may provide a greater therapeutic effect for accommodative and binocular vision disorders than center near designs because the central portion of the lens is the addition power, unlike the center-distance lens designs. This study will aim to determine how accommodative function varies with center distance and center near multifocal contact lenses.


Recruitment information / eligibility

Status Recruiting
Enrollment 20
Est. completion date December 31, 2024
Est. primary completion date December 31, 2024
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 30 Years
Eligibility Inclusion Criteria: - Ages 18 to = 30 years old - Acuity of 20/25 or better in both eyes with habitual contact lens prescription - No history of ocular disease or active ocular inflammation - No history of ocular or refractive surgery - No current history of rigid contact lens wear - Astigmatism =1.00 D - Free of binocular vision disorder (strabismus, amblyopia, vergence dysfunction, accommodative dysfunction) Exclusion Criteria: - No prior or concurrent participation in myopia control or use of low dose atropine, multifocal contact lenses - No use of any medications suspected to affect accommodation

Study Design


Related Conditions & MeSH terms


Intervention

Device:
Contact Lens
Coopervision Biofinity Multifocal Lens

Locations

Country Name City State
United States The Ohio State University Columbus Ohio

Sponsors (1)

Lead Sponsor Collaborator
Ohio State University

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Objective Accommodative Outcome Accommodative function will be compared using the Grand Seiko Autorefractor between the center distance and center near group. The instrument will record the patient's refractive error at distance and near (100 cm, 40 cm, and 25 cm) Up to two hours
Secondary Accommodation Clinical Measures Accommodation will be assessed with monocular estimation method which is done with a clinical retinoscope, accommodative facility which uses lenses to determine how many times a patient can clear a target in one minute, and monocular accommodative push ups which is measured by bringing a reading target close to the eye and the patient reports when the target gets blurry. These eye focusing tests and outcomes will be compared in center distance and center near multifocal contact lens designs. Up to two hours
Secondary Vergence Clinical Measures Vergence measures will be completed by checking cover test, which an examiner determines eye posture with a cover paddle and a near target. Modified Thorington will be assessed at distance and near, which is a card with a light in the center. The patient holds up a red lens over their eye and they report where they see the line crossing the cards. Up to two hours
See also
  Status Clinical Trial Phase
Completed NCT04297969 - Hyperopia Detection GCK With Glow Fixation
Withdrawn NCT05107791 - Effects of Stulln and Accommodative Training Phase 1/Phase 2
Recruiting NCT06331780 - Refractive Status and Accommodation Response Under Different Experimental Conditions. N/A
Recruiting NCT06286410 - Accommodation Response in Hypermetropic Anisometropia (ARIHA Study) N/A
Active, not recruiting NCT03906279 - Choroidal Thickness Change in Response to Physiological and Refractive Changes