- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00494390
Evaluation Study for a Non-Contact Biometer
March 18, 2008 updated by: University Hospital Inselspital, Berne
Neuartige Kontaktlose Biometrische Messungen
The purpose of this study is to determine whether a new non-contact biometer, is as accurate as the the available gold-standard.
Study Overview
Status
Completed
Conditions
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 Type
Observational
Enrollment (Anticipated)
95
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
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Bern, Switzerland, 3010
- Department of Ophthalmology, University Hospital
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Description
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)
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Collaborators
Investigators
- Principal Investigator: David Goldblum, MD, www.insel.ch
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
July 1, 2007
Primary Completion (Actual)
March 1, 2008
Study Registration Dates
First Submitted
June 27, 2007
First Submitted That Met QC Criteria
June 27, 2007
First Posted (Estimate)
June 29, 2007
Study Record Updates
Last Update Posted (Estimate)
March 19, 2008
Last Update Submitted That Met QC Criteria
March 18, 2008
Last Verified
July 1, 2007
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- kek-98/07
- Insel 1351
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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