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Evaluation Study for a Non-Contact Biometer

Neuartige Kontaktlose Biometrische Messungen

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT00494390
Enrollment
95
Registered
2007-06-29
Start date
2007-07-31
Completion date
Unknown
Last updated
2008-03-19

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Aphakia, Cataract, Hyperopia, Myopia, Pseudophakia

Keywords

Biometry, corneal opacity, astigmatism, refraction

Brief summary

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

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.

Interventions

None listed

Sponsors

Haag-Streit AG
CollaboratorINDUSTRY
Insel Gruppe AG, University Hospital Bern
Lead SponsorOTHER

Study design

Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

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)

Countries

Switzerland

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026