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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00494390
Other study ID # kek-98/07
Secondary ID Insel 1351
Status Completed
Phase N/A
First received June 27, 2007
Last updated March 18, 2008
Start date July 2007

Study information

Verified date July 2007
Source University Hospital Inselspital, Berne
Contact n/a
Is FDA regulated No
Health authority Switzerland: EthikkommissionSwitzerland: Laws and standardsSwitzerland: Swissmedic
Study type Observational

Clinical Trial Summary

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


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.


Recruitment information / eligibility

Status Completed
Enrollment 95
Est. completion date
Est. primary completion date March 2008
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 18 Years and older
Eligibility 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)

Study Design

Time Perspective: Prospective


Related Conditions & MeSH terms


Locations

Country Name City State
Switzerland Department of Ophthalmology, University Hospital Bern

Sponsors (2)

Lead Sponsor Collaborator
University Hospital Inselspital, Berne Haag-Streit International

Country where clinical trial is conducted

Switzerland, 

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