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Study of Clinical Performance of Corneal Topography Measurement Using an Optical Biometer

H

Haag-Streit

Status

Completed

Conditions

Corneal Topography

Study type

Observational

Funder types

Other
Industry

Identifiers

NCT01861925
HS-LS900-TOPO-01

Details and patient eligibility

About

The purpose of this study is to quantify in-vivo repeatability of a new corneal topography measurement mode of an optical biometer, and the clinical performance of measurement in comparison to reference devices.

Enrollment

50 patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • 18 years or older

Exclusion criteria

  • No corneal transplants
  • No corneal scar(s)
  • No acute infections of the eye
  • No weak fixation
  • No suspected lack of compliance
  • No vulnerable population

Trial design

50 participants in 3 patient groups

Normal eye
Description:
Astigmatism smaller than 1.5 diopters
Large regular astigmatism
Description:
Astigmatism of \> 1.5 diopters, regular astigmatism.
Large irregular astigmatism
Description:
Astigmatism of \> 1.5 diopters, irregular astigmatism.

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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