Evaluation Study for a Non-Contact Biometer
Sponsor
University Hospital Inselspital, Berne (Other)
Overall Status
Completed
CT.gov ID
NCT00494390
Collaborator
Haag-Streit AG (Industry)
95
1
Study Details
Study Description
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.
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
|
|
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 Design
Study Type:
Observational
Anticipated Enrollment
:
95 participants
Time Perspective:
Prospective
Official Title:
Neuartige Kontaktlose Biometrische Messungen
Study Start Date
:
Jul 1, 2007
Actual Primary Completion Date
:
Mar 1, 2008
Outcome Measures
Primary Outcome Measures
Eligibility Criteria
Criteria
Ages Eligible for Study:
18 Years
and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
-
18 year or older
-
Normal eye
-
Cataract
-
Corneal abnormality (scar, opacity, transplant)
-
refractive corneal surgery
-
Pseudophakia
-
Aphakia
-
Silicon oil
-
refractive IOL
2.-9. (at least one yes)
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | Department of Ophthalmology, University Hospital | Bern | Switzerland | 3010 |
Sponsors and Collaborators
- University Hospital Inselspital, Berne
- Haag-Streit AG
Investigators
- Principal Investigator: David Goldblum, MD, www.insel.ch
Study Documents (Full-Text)
None provided.More Information
Publications
None provided.Responsible Party:
,
,
ClinicalTrials.gov Identifier:
NCT00494390
Other Study ID Numbers:
- kek-98/07
- Insel 1351
First Posted:
Jun 29, 2007
Last Update Posted:
Mar 19, 2008
Last Verified:
Jul 1, 2007
Keywords provided by ,
,
Additional relevant MeSH terms: