A Study to Evaluate Base-in Prism Spectacles for Intermittent Exotropia

Overview

About this study

The purpose of this study is to compare spectacles with relieving prism to spectacles without prism to determine whether to proceed to a full-scale, longer-term randomized trial. This decision will be based primarily on assessing the initial (8-week) response to prism by comparing treatment groups on the following outcomes: 

  • Mean distance intermittent exotropia (IXT) control score (the mean of 3 control scores) (primary outcome);
  • The proportion of participants demonstrating a "treatment response," defined as ≥ 1 point improvement in the mean distance IXT control score without spontaneous exotropia during control testing (secondary outcome);
  • The proportion of participants reporting adverse effects and good/excellent spectacle wear compliance.

Participation eligibility

Participant eligibility includes age, gender, type and stage of disease, and previous treatments or health concerns. Guidelines differ from study to study, and identify who can or cannot participate. There is no guarantee that every individual who qualifies and wants to participate in a trial will be enrolled. Please contact the study team to discuss whether or not you are eligible to participate in a study.

Inclusion Criteria:

  • Age 3 to 13 years old.
  • Mean distance control score of ≥2.00 points with at least 1 measure of 3, 4, or 5 points (i.e, spontaneous tropia) from the 3 assessments during the exam.
  • A near control score ≤ 4 on at least 1 of 3 assessments (cannot have score of 5, 5, 5). 
  • Distance exodeviation between 16 Prism Diopters (Δ) and 35 Δ (inclusive) by PACT.
  • Near exodeviation between 10 Δ and 35 Δ (inclusive) by PAC.T 
  • Near deviation does not exceed distance deviation by more than 10 Δ by PACT (i.e., convergence insufficiency-type IXT excluded) - Refractive error between -6.00 Diopters (D) spherical equivalent (SE) and +2.50 D SE (inclusive) (based on a cycloplegic refraction performed within 7 months but prior to the day of enrollment).
  • Refractive correction (must be worn for at least 1 week if refractive error meets any of the following (based on a cycloplegic refraction performed within 7 months but prior to the day of enrollment): 
    • SE anisometropia ≥ 1.00 D;
    • Astigmatism ≥ 1.00 D in either eye;
    • SE myopia ≥ -0.50 D in either eye.
  • If spectacles have been prescribed and are worn, they must meet the following pre- enrollment criteria:
    • SE anisometropia corrected to within 1.00 D of full SE anisometropic difference; 
    • Astigmatism corrected to within 1.00 D of full magnitude; axis within 10 degrees if astigmatism ≤ 1.00 D and axis within 5 degrees if astigmatism > 1.00 D.

Exclusion Criteria:

  • Dissociated vertical deviation (DVD).
  • Vertical deviation > 3 Δ in primary gaze at distance or near.
  • Patterns (such as an "A" or "V" pattern) with a downgaze measurement of >10 Δ difference from straight ahead by PACT, measured per investigator's routine method.
  • Treatment for IXT or amblyopia (other than refractive correction) within the past 4 weeks, including vision therapy, orthoptics, patching, atropine, or other penalization.
  • Substantial overminus spectacles (spectacles overminused by more than 1.00 D SE than the most recent cycloplegic refraction and also results in minus SE power in the spectacles; underplussing is allowed) within the past 4 weeks.
  • Prior strabismus, intraocular, or refractive surgery (including BOTOX injection).
  • Previous use of prism spectacles Additional Eligibility Criteria for Randomization Based on Prism Adaptation Testing - Exodeviation by PACT while wearing "trial" relieving prism for 30 minutes is smaller at distance or near than measured during initial testing. (e.g. not fully adapting to prism at both distances).
  • No new esotropia on cover test at near while wearing "trial" relieving prism for 30 minutes, compared with enrollment measurement taken without prism.
  • No esodeviation >6 Δ on PACT at near while wearing "trial" relieving prism for 30 minutes.

Participating Mayo Clinic locations

Study statuses change often. Please contact the study team for the most up-to-date information regarding possible participation.

Mayo Clinic Location Status Contact

Rochester, Minn.

Mayo Clinic principal investigator

Jonathan Holmes, M.D.

Open for enrollment

Contact information:

Suzanne Wernimont CCRP

(507)293-5060

Wernimont.Suzanne@mayo.edu

More information

Publications

Publications are currently not available

Study Results Summary

Not yet available

Supplemental Study Information

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CLS-20470197

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