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Analysis of Clinical Profiles of Chinese Patients With Normal Tension Glaucoma

This study is currently recruiting participants.
Verified by Chinese University of Hong Kong, May 2008

Sponsors and Collaborators: Chinese University of Hong Kong
Hong Kong Eye Hospital
Prince of Wales Hospital, Shatin, Hong Kong
Information provided by: Chinese University of Hong Kong
ClinicalTrials.gov Identifier: NCT00321386
  Purpose

To obtain demographic and baseline ophthalmic parameters (such as Intraocular Pressure profiles, disc morphological characteristics, central corneal thickness, peripapillary retinal nerve fibre layer thickness and its serial changes, visual field changes, severity of any medical associations—e.g. hypertension, migraine, strokes) with non-invasive measurements, in Chinese Patients with Normal Tension Glaucoma


Condition
Glaucoma

Genetics Home Reference related topics:   early-onset glaucoma   

MedlinePlus related topics:   Glaucoma   

U.S. FDA Resources

Study Type:   Observational
Study Design:   Cohort, Prospective
Official Title:   Parameters for Disease Progression in Chinese Patients With Normal Tension Glaucoma

Further study details as provided by Chinese University of Hong Kong:

Biospecimen Retention:   Samples With DNA

Biospecimen Description:

Blood taking for glaucoma genetics analysis shall be performed.


Estimated Enrollment:   500
Study Start Date:   December 2003
Estimated Study Completion Date:   December 2009
Estimated Primary Completion Date:   December 2008 (Final data collection date for primary outcome measure)

Show detailed description  Show Detailed Description

  Eligibility
Ages Eligible for Study:   18 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   Yes
Sampling Method:   Non-Probability Sample

Study Population

Patients with Normal Tension Glaucoma recruited from a teritary University Eye Hospital setting.


Criteria

Inclusion Criteria:

  • All Chinese patients with age>18 years old with Normal Tension Glaucoma will be recruited

Exclusion Criteria:

  • Diseases that precluded accurate measurement of IOP, visual acuity, retinal nerve fiber layer thickness, and visual field tests.
  • Previous ocular surgery per se is not an exclusion criteria.
  Contacts and Locations

Please refer to this study by its ClinicalTrials.gov identifier: NCT00321386

Contacts
Contact: LEUNG YL Dexter, MBChB, FRCS     852-27623000     dexleung@alumni.cuhk.net    

Locations
Hong Kong
Hong Kong Eye Hospital     Recruiting
      Hong Kong, Hong Kong
      Contact: LEUNG YL Dexter, MBChB, FRCS     852-27623000     dexleung@alumni.cuhk.net    
      Sub-Investigator: THAM CY Clement, MA, MD, FRCS            
Prince of Wales Hospital     Recruiting
      Hong Kong, Hong Kong

Sponsors and Collaborators
Chinese University of Hong Kong
Hong Kong Eye Hospital
Prince of Wales Hospital, Shatin, Hong Kong

Investigators
Principal Investigator:     LEUNG YL Dexter, MBChB, FRCS     Glaucoma Service, Hong Kong Eye Hospital    
Study Chair:     LAM SC Dennis, MD, FRCOphth     Chinese University of Hong Kong    
  More Information


Publications:

Responsible Party:   Department of Ophthalmology & Visual Sciences, The Chinese University of HK ( Dr. Dexter Leung/ Honorary Clinical Assistant Professor )
Study ID Numbers:   KC/KE 05-0169/ER-1, CRE-2005.434
First Received:   May 1, 2006
Last Updated:   May 13, 2008
ClinicalTrials.gov Identifier:   NCT00321386
Health Authority:   Hong Kong: Ethics Committee

Keywords provided by Chinese University of Hong Kong:
Glaucoma  
Open Angle  
Normal Tension  

Study placed in the following topic categories:
Glaucoma
Eye Diseases
Disease Progression
Hypertension
Ocular Hypertension

ClinicalTrials.gov processed this record on November 06, 2008




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