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Validation of the GATE Software (ValGATE)

U

University Hospital Tuebingen

Status

Completed

Conditions

Visual Field Defects

Treatments

Procedure: perimetry

Study type

Observational

Funder types

Other
Industry

Identifiers

NCT01265628
161/2009BO2 (Other Identifier)
HSC GATE Strategie

Details and patient eligibility

About

Comparison of the differential luminance sensitivity (DLS) values at each test point

Enrollment

30 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • physical, intellectual and linguistic abilities, in order to understand the test requirements
  • spherical ametropia max. ± 8 dpt, cylindrical ametropia max. ± 3 dpt
  • distant visual acuity > 10/20
  • isocoria, pupil diameter > 3 mm

Exclusion criteria

  • pregnancy, nursing
  • diabetic retinopathy
  • asthma
  • HIV+ or AIDS
  • history of epilepsy or significant psychiatric disease
  • medications known to effect visual field sensitivity
  • acute ocular infections (e.g. keratitis, conjunctivitis, uveitis)
  • severe dry eyes
  • miotic drugs
  • amblyopia
  • squint
  • nystagmus
  • albinism
  • keratoconus
  • intraocular surgery (except for uncomplicated cataract surgery) performed < 3 month prior to screening
  • history or presence of macular disease and / or macular edema
  • relevant opacities of central refractive media (cornea, lens, vitreous body)
  • ocular trauma

Trial design

30 participants in 3 patient groups

Glaucoma
Treatment:
Procedure: perimetry
Retinitis pigmentosa (RP)
Treatment:
Procedure: perimetry
Anterior Ischemic Optic Neuropathy (AION)
Treatment:
Procedure: perimetry

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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