A Study of Clinical Characteristics, Treatments, and One-Year Outcomes of Adults with Strabismus

Overview

Información sobre este estudio

The purpose of this study is to describe clinical characteristics, treatments, and one-year outcomes for adults who have convergence insufficiency, divergence insufficiency, or small angle hypertropia.

Elegibilidad para la participación

Los requisitos de elegibilidad de los participantes incluyen la edad, el sexo, el tipo y el estadio de la enfermedad, y los problemas de salud o tratamientos previos. Las pautas difieren de un estudio a otro e identifican quiénes pueden o no pueden participar. No hay garantía de que cada persona elegible que desee participar en un ensayo se inscribirá. Comunícate con el equipo del estudio para analizar la elegibilidad del estudio y la posible participación.

Inclusion Criteria 

  • Convergence Insufficiency Group
    • Adults ≥18 years of age (adult onset of CI not required)
    • No strabismus surgery within the past 10 years
    • CI Symptom Survey score ≥ 21 points
    • Near exodeviation of ≥4∆ and at least 4∆ larger than at distance by PACT
    • Distance exodeviation ≤15∆ by PACT
    • Vertical deviation ≤2∆ at distance and near by PACT
    • No constant exotropia at distance or near
    • Reduced positive fusional vergence (PFV) at near (<20∆ or fails Sheard's criterion that the PFV measures less than twice the magnitude of the near phoria)
    • Near point of convergence of ≥ 6 cm break
    • Visual acuity 20/50 or better in both eyes by ETDRS or Snellen
    • No paralytic strabismus (e.g., 3rd, 4th, or 6th cranial nerve palsies, skew deviation, Duane syndrome)
    • No restrictive strabismus (e.g., blowout fracture, thyroid eye disease, post scleral buckle, Brown syndrome)
    • No monocular diplopia
    • No paretic strabismus, thyroid eye disease, myasthenia gravis, chronic progressive external ophthalmoplegia, or eye movement abnormalities associated with known neurological disease. Patients with Parkinson's disease can be enrolled if non-paretic deviation
    • No inferior or superior oblique overaction defined as 2+ or greater
    • Ability to fuse with prism in space 
    • Ability to understand and complete a survey
    • Investigator is initiating treatment with prism, orthoptic exercises, botulinum toxin injection or surgery
    • If initiating treatment with botulinum toxin or surgery, planned injection or surgery to be within 60 days of enrollment
    • Single treatment modality is planned (e.g., no combined prism and orthoptic exercises)
    • Treatment to be initiated has not been used within the past one year
  • Divergence Insufficiency Group
    • Adults ≥18 years of age
    • Adult-onset Divergence insufficiency at ≥ 18 years of age
    • No prior strabismus surgery
    • Symptoms of diplopia at distance with a frequency of sometimes or worse in primary position (in current glasses if wearing glasses)
    • Distance esodeviation of 2∆ to 30∆ and at least 50% larger than at near by PACT
    • No more than 5∆ difference between right and left gaze by PACT
    • No more than 10∆ difference between the primary position at distance and either upgaze or downgaze ≤10∆ by PACT
    • Any coexisting vertical deviation must be less than distance esodeviation and ≤10∆ by PACT
    • Visual acuity 20/50 or better in both eyes by ETDRS or Snellen
    • No paralytic strabismus (e.g., 3rd, 4th, or 6th cranial nerve palsies, skew deviation, Duane syndrome)
    • No restrictive strabismus (e.g., blowout fracture, thyroid eye disease, post scleral buckle, Brown syndrome)
    • No monocular diplopia
    • No paretic strabismus, thyroid eye disease, myasthenia gravis, chronic progressive external ophthalmoplegia, or eye movement abnormalities associated with known neurological disease
      • Parkinson's disease can be enrolled if non-paretic deviation
    • No inferior or superior oblique overaction defined as 2+ or greater
    • Ability to fuse with prism in space 
    • Ability to understand and complete a survey
    • Investigator is initiating treatment with prism, orthoptic exercises, botulinum toxin injection or surgery
    • If treatment with botulinum toxin or surgery, planned injection or surgery to be within 60 days of enrollment
    • Single treatment modality planned (e.g., no combined prism and orthoptic exercises)
    • Treatment to be initiated has not been used within the past one year
  • Small-angle Hypertropia Group
    • Adults ≥18 years of age
    • Adult-onset HT (at ≥18 years of age)
    • No prior strabismus surgery
    • Symptoms of diplopia at distance or near with a frequency of sometimes or worse in primary or reading position (in current glasses if wearing glasses)
    • Vertical deviation ≥1∆ to ≤10∆ at distance and near by PACT
    • No more than 4∆ difference from the primary in any gaze position by PACT
    • Any coexisting esodeviation must be less than the vertical deviation
    • Any coexisting exodeviation ≤10∆ by PACT
    • No convergence insufficiency
    • Visual acuity 20/50 or better in both eyes by ETDRS or Snellen
    • No paralytic strabismus (e.g., 3rd, 4th, or 6th cranial nerve palsies, skew deviation, Duane syndrome)
    • No restrictive strabismus (e.g., blowout fracture, thyroid eye disease, post scleral buckle, Brown syndrome)
    • No monocular diplopia
    • No paretic strabismus, thyroid eye disease, myasthenia gravis, chronic progressive external ophthalmoplegia, or eye movement abnormalities associated with known neurological disease
      • Parkinson's disease can be enrolled if of non-paretic deviation
    • No inferior or superior oblique overaction defined as 2+ or greater
    • Ability to fuse with prism in space
    • Ability to understand and complete a survey
    • Investigator is initiating treatment with prism, orthoptic exercises, botulinum toxin injection or surgery
    • If initiating treatment with botulinum toxin or surgery, planned injection or surgery to be within 60 days of enrollment
    • Single treatment modality planned (e.g., no combined prism and orthoptic exercises)
    • Treatment to be initiated has not been used within the past one year

Sedes participantes de Mayo Clinic

Los estatus de los estudios cambian con frecuencia. Comunícate con el equipo del estudio para obtener la información más actualizada acerca de la posibilidad de participar.

Sede de Mayo Clinic Estatus

Rochester, Minn.

Investigador principal de Mayo Clinic

Erick Bothun, M.D.

Cerrado para la inscripción

More information

Publicaciones

Publications are currently not available
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CLS-20264110

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