- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00863876
Comparison of WaveLight Analyzer and Alcon LadarWave
June 28, 2010 updated by: WaveLight AG
Comparison of repeated WaveLight Analyzer and Alcon LadarWave measurements in phakic and pseudophakic eyes.
Study Overview
Status
Completed
Conditions
Study Type
Observational
Enrollment (Anticipated)
144
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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Heidelberg, Germany, 69120
- University of Heidelberg, Dept. of Ophthalmology
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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
Study Population
healthy patients and patients following surgery, patients with keratoconus presenting for examination at the clinic
Description
Inclusion Criteria:
- healthy eyes or eyes with the study conditions
Exclusion Criteria:
- age < 18, eye disorders other than mentioned above, participation in any other study,
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
Cohorts and Interventions
Group / Cohort |
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1
non-operated healthy eyes
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2
eyes 1 months following LASIK
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3
eyes 3-6 months following LASIK
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4
eyes with spherical monofocal IOLs more than 3 months postop
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5
eyes with aspherical monofocal IOLs more than 3 months postop
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6
eyes with toric monofocal IOLs more than 3 months postop
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7
eyes with diffractive multifocal IOLs more than 3 months postop
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8
eyes with phakic IOLs more than 3 months postop
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9
eyes with keratoconus
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
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
March 1, 2009
Study Registration Dates
First Submitted
March 17, 2009
First Submitted That Met QC Criteria
March 17, 2009
First Posted (Estimate)
March 18, 2009
Study Record Updates
Last Update Posted (Estimate)
June 29, 2010
Last Update Submitted That Met QC Criteria
June 28, 2010
Last Verified
June 1, 2010
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- S-388/2008
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.