Evaluation Study for a Non-Contact Biometer
Neuartige Kontaktlose Biometrische Messungen
2 other identifiers
observational
95
1 country
1
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.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
June 27, 2007
CompletedFirst Posted
Study publicly available on registry
June 29, 2007
CompletedStudy Start
First participant enrolled
July 1, 2007
CompletedPrimary Completion
Last participant's last visit for primary outcome
March 1, 2008
CompletedMarch 19, 2008
July 1, 2007
8 months
June 27, 2007
March 18, 2008
Conditions
Keywords
Eligibility Criteria
You may qualify if:
- year or older
- Normal eye
- Cataract
- Corneal abnormality (scar, opacity, transplant)
- refractive corneal surgery
- Pseudophakia
- Aphakia
- Silicon oil
- refractive IOL
- (at least one yes)
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Insel Gruppe AG, University Hospital Bernlead
- Haag-Streit AGcollaborator
Study Sites (1)
Department of Ophthalmology, University Hospital
Bern, 3010, Switzerland
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
David Goldblum, MD
www.insel.ch
Study Design
- Study Type
- observational
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
Study Record Dates
First Submitted
June 27, 2007
First Posted
June 29, 2007
Study Start
July 1, 2007
Primary Completion
March 1, 2008
Last Updated
March 19, 2008
Record last verified: 2007-07