Evaluation Study for a Non-Contact Biometer

Overview

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

Full Title of Study: “Neuartige Kontaktlose Biometrische Messungen”

Study Type

  • Study Type: Observational
  • Study Design
    • Time Perspective: Prospective
  • Study Primary Completion Date: March 2008

Detailed 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.

Participating in This Clinical Trial

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)

Gender Eligibility: All

Minimum Age: 18 Years

Maximum Age: N/A

Are Healthy Volunteers Accepted: Accepts Healthy Volunteers

Investigator Details

  • Lead Sponsor
    • Insel Gruppe AG, University Hospital Bern
  • Collaborator
    • Haag-Streit AG
  • Overall Official(s)
    • David Goldblum, MD, Principal Investigator, www.insel.ch

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