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The contribution of race as a determining factor in the development of glaucoma
ISRCTN ISRCTN09311359
ClinicalTrials.gov identifier
Public title The contribution of race as a determining factor in the development of glaucoma
Scientific title The contribution of race as a determining factor in the development of Primary Open Angle Glaucoma (POAG): An observational trial
Acronym ADS (aqueous dynamic study)
Serial number at source N/A
Study hypothesis The distribution of aqueous production rate and the out-flow facility in patients from different racial groups with POAG.

Primary open angle glaucoma is defined as glaucomatous optic neuropathy together with an IOP >21 mmHg on at least one occasion and visual field defects (using the 24-2 test pattern on a Humphrey Field Analyzer) and a gonioscopic angle width of 3 or 4 and normal in appearance.
Ethics approval St. Thomas' Hospital Research Ethics Committee, Approved on 14 August 2007, REC ref number: 07/Q0702/61
Study design Prospective observational longitudinal non-randomised study
Countries of recruitment United Kingdom
Disease/condition/study domain Primary open angle glaucoma (POAG)
Participants - inclusion criteria 1. Males or Females between ages 18 and 90
2. Availability to participate in all aspects of the study
3. Willingness to participate in a study
4. Ability to undergo accurate fluorophotometry and tonography
Participants - exclusion criteria 1. History of intraocular surgery or keratorefractive surgery
2. Systemic medications which affects aqueous production, such as beta adrenergic blockers, steroids
3. Fluorescein allergy
Anticipated start date 15/10/2007
Anticipated end date 31/05/2010
Status of trial Completed
Patient information material Not available in web format, please use contact details below to request a patient information sheet
Target number of participants 30 patients from each of the following race groups with or without POAG: African origin and White Caucasian
Interventions Patients will receive standard treatment and care. Therefore, there is no intervention, just some extra measurements which used to be part of routine clinical examinations.
Additional measurements will be carried out using pnuematonometry, fluorophotometry and Schiotz tonography machines
Primary outcome measure(s) Outflow facility determined
Comparison of results before and 3 months after treatment
Secondary outcome measure(s) 1. Anterior chamber depth
2. Intraocular pressure
Comparison of results before and 3 months after treatment
Sources of funding Eye Hope Charity (UK)
Trial website
Publications
Contact name Mr  Kin Sheng   Lim
  Address St. Thomas' Hospital
Westminster Bridge Road
  City/town London
  Zip/Postcode SE1 7EH
  Country United Kingdom
  Tel +44 (0)20 7188 2289
  Fax +44 (0)20 7188 4318
  Email shenglim@gmail.com
Sponsor Guy's and St. Thomas NHS Foundation Trust (UK)
  Address c/o Karen Ignatian
Research and Development
3rd Floor Conybeare House
Guy's House
Guy's Hospital
St .Thomas Street
  City/town London
  Zip/Postcode SE1 9RT
  Country United Kingdom
  Tel +44 (0)20 7188 5731
  Fax +44 (0)20 7188 5434
  Email karen.ignatian@gstt.nhs.uk
  Sponsor website: http://www.guysandstthomas.nhs.uk/
Date applied 07/12/2009
Last edited 02/02/2010
Date ISRCTN assigned 02/02/2010
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