- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01546740
Prevalence of Glaucoma in the Israeli Arab Population
March 6, 2012 updated by: Ziv Hospital
Glaucoma Prevalence in the Israeli Arab Population
there is a variety of glaucoma prevalence within different populations.
this study examine the prevalence of glaucoma in the Arab population in Israel' as well as the demographic variables and the compliance to treatment in the population.
Study Overview
Status
Unknown
Conditions
Detailed Description
from Medical records of primary care clinic in the city of Tira. the patients are recruited, all glaucoma patients are above age of 20 years.
they must suffer from CDR >= 0.5 with/without asymmetry with the other eye.
or they suffer from glaucomatous damage to the visual fields.
Study Type
Observational
Enrollment (Anticipated)
15000
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Joseph Pikkel, M.D
- Phone Number: +972508434206
- Email: pikel.y@ziv.health.gov.il
Study Contact Backup
- Name: Otzem Chassid, M.D
- Phone Number: +972506266059
- Email: otzem.c@ziv.health.gov.il
Study Locations
-
-
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Safed, Israel, 13120
- Recruiting
- Ziv Medical Center
-
Contact:
- Joseph Pikkel, M.D
- Phone Number: +972508434206
- Email: pikel.y@ziv.health.gov.il
-
Contact:
- Otzem Chassid, M.D
- Phone Number: +972506266059
- Email: otzem.c@ziv.health.gov.il
-
-
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
20 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
primary care clinics from 1 Arab city in the center of Israel
Description
Inclusion Criteria:
- Cup-to-disk ratio (CDR) > 0.5 with asymmetry between the eyes
- Intraocular pressure (IOP) > 23 mm Hg
- Damage to the field of vision
- Age- above 20 Yrs. old
Exclusion Criteria:
- None
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 |
---|
Glaucoma patients
all the ,medical records of patients who were diagnosed with primary open angle glaucoma, closed angle , pseudoexfoliative and neovascular glaucoma.
|
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
January 1, 2012
Primary Completion (Anticipated)
April 1, 2012
Study Completion (Anticipated)
May 1, 2012
Study Registration Dates
First Submitted
March 1, 2012
First Submitted That Met QC Criteria
March 6, 2012
First Posted (Estimate)
March 7, 2012
Study Record Updates
Last Update Posted (Estimate)
March 7, 2012
Last Update Submitted That Met QC Criteria
March 6, 2012
Last Verified
March 1, 2012
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- ZIV-0060-11
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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