- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01067482
The Performances of Spectral Domain Optical Coherence Tomography (OCT) for Distinguishing Glaucomatous Eyes (cirrusOCT)
March 22, 2010 updated by: Prince of Songkla University
The Performances of Spectral Domain Optical Coherence Tomography for Distinguishing Between Normal Eyes, Glaucoma Suspect and Glaucomatous Eyes
The purpose of this study is to evaluate performances of each parameters of spectral domain (Cirrus) optical coherence tomography for distinguishing between normal eyes, glaucoma suspect and glaucomatous eyes
Study Overview
Status
Completed
Detailed Description
Aim to determine which parameter of cirrus OCT is best sensitivity and specificity for glaucoma detection
Study Type
Observational
Enrollment (Anticipated)
80
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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Songkhla, Thailand.
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Hat-yai,, Songkhla, Thailand., Thailand, 90110
- Glaucoma unit , Department of Ophthalmology Faculty of Medicine Prince of Songkla University
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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 to 80 years (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Probability Sample
Study Population
glaucoma patient from glaucoma clinic that is POAG Glaucoma suspect cases normal population case
Description
Inclusion Criteria:
- BCVA at least 20/60
- refractive error +/- 5 D Or astig +/- 3 D
- enrolled in 3 population group (glaucoma, glaucoma suspect or normal)
Exclusion Criteria:
- VA less than 20/60
- marked RF error
- previous ocular trauma or surgery
- unreliable visual field
- poor signal cirrus OCT (less than 7)
- other causes of optic nerve or macular disease other than glaucoma
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
- Time Perspectives: Prospective
Cohorts and Interventions
Group / Cohort |
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Glaucoma patients
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Glaucoma suspect group
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Normal population
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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
September 1, 2009
Primary Completion (Actual)
March 1, 2010
Study Completion (Actual)
March 1, 2010
Study Registration Dates
First Submitted
February 10, 2010
First Submitted That Met QC Criteria
February 10, 2010
First Posted (Estimate)
February 11, 2010
Study Record Updates
Last Update Posted (Estimate)
March 23, 2010
Last Update Submitted That Met QC Criteria
March 22, 2010
Last Verified
October 1, 2009
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- EC 52-336-02-1-2
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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