Evaluation Study for a Non-Contact Biometer

Completed

• Conditions: Cataract; Pseudophakia; Myopia; Hyperopia; Aphakia

• Registration Number: NCT00494390
• Lead Sponsor: Insel Gruppe AG, University Hospital Bern

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.

Study Timeline

• Study First Submitted: 2007-06-27
• Study First Submitted QC: 2007-06-27
• Study First Posted: 2007-06-29
• Status Verified: 2007-07
• Study Start: 2007-07
• Primary Completion: 2008-03
• Last Update Submitted: 2008-03-18
• Last Update Posted: 2008-03-19

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 95

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)

Exclusion Criteria

Not provided

Study & Design

• Study Type: OBSERVATIONAL
• Study Design: Not specified

Trial Locations

Locations (1)

Department of Ophthalmology, University Hospital; 🇨🇭 Bern, Switzerland