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Evaluation Study for a Non-Contact Biometer

I

Insel Gruppe AG, University Hospital Bern

Status

Completed

Conditions

Myopia
Pseudophakia
Cataract
Aphakia
Hyperopia

Study type

Observational

Funder types

Other
Industry

Identifiers

NCT00494390
kek-98/07
Insel 1351

Details and patient eligibility

About

The purpose of this study is to determine whether a new non-contact biometer, is as accurate as the the available gold-standard.

Full description

The features of a not yet commercial available new biometer will be compared to available contact and non contact biometers in different patient groups.

Enrollment

95 estimated patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria:

  1. 18 year or older
  2. Normal eye
  3. Cataract
  4. Corneal abnormality (scar, opacity, transplant)
  5. refractive corneal surgery
  6. Pseudophakia
  7. Aphakia
  8. Silicon oil
  9. refractive IOL

2.-9. (at least one yes)

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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