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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