Eligibility Module

Eligibility Module

The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.

Eligibility Module path is as follows:

Study -> Protocol Section -> Eligibility Module

Eligibility Module


Ignite Creation Date: 2025-12-25 @ 5:06 AM
Ignite Modification Date: 2025-12-25 @ 5:06 AM
NCT ID: NCT04691427
Eligibility Criteria: Inclusion Criteria: * Age 9 years and older * CISS score ≥ 16 * Best-corrected distance visual acuity of 20/25 or better in each eye * Random dot stereopsis appreciation of 500 seconds of arc or better * Parent or subject understands the protocol and is willing to enroll in the study Exclusion Criteria: * Constant strabismus at distance or near * Vertical heterophoria ≥ 2 ∆ at distance or near * ≥ 2 line interocular difference in best-corrected visual acuity * Near point of accommodation \> 20 cm in either eye as measured by push-up method * Manifest or latent nystagmus * Non-strabismic binocular vision and accommodative disorders associated with known disease of the brain * Diseases known to affect accommodation, vergence, or ocular motility such as multiple sclerosis, Graves orbitopathy, myasthenia gravis, diabetes mellitus, Parkinson disease * Any ocular or systemic medication known to affect accommodation or vergence such as anti-anxiety agents (e.g., Librium or Valium), anti-arrhythmic agents (e.g., Cifenline, Cibenzoline), anti-cholinergics, bladder spasmolytic drugs (e.g., Propiverine), hydroxychloroquine, chloroquine, phenothiazines (e.g., Compazine, Mellaril, Thorazine), tricyclic antidepressants (e.g., Elavil, Nortriptyline, Tofranil) * Inability to comprehend and/or perform any study-related test or procedure
Healthy Volunteers: False
Sex: ALL
Minimum Age: 9 Years
Maximum Age: 35 Years
Study: NCT04691427
Study Brief:
Protocol Section: NCT04691427