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Trial details imported from ClinicalTrials.gov
For full trial details, please see the original record at
https://clinicaltrials.gov/study/NCT00150267
Registration number
NCT00150267
Ethics application status
Date submitted
6/09/2005
Date registered
8/09/2005
Date last updated
5/11/2008
Titles & IDs
Public title
A 5-Year Postmarketing Safety Study Of Xalcom In Patients With Open Angle Glaucoma Or Ocular Hypertension
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Scientific title
A 5-Year Postmarketing Safety Study Of Xalcom In Patients With Open Angle Glaucoma Or Ocular Hypertension
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Secondary ID [1]
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912-OPT-0076-019
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Universal Trial Number (UTN)
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Trial acronym
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Linked study record
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Health condition
Health condition(s) or problem(s) studied:
Glaucoma, Open-Angle
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Ocular Hypertension
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Condition category
Condition code
Eye
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Diseases / disorders of the eye
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Cardiovascular
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0
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Hypertension
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
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Comparator / control treatment
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Control group
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Outcomes
Primary outcome [1]
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Incidence of increase of iris pigmentation
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Assessment method [1]
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Timepoint [1]
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Primary outcome [2]
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incidence of development in darkening/lengthening/thickening of eyelashes and/or pigmentation of periorbital skin
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Assessment method [2]
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Timepoint [2]
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Primary outcome [3]
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occurrence of ocular/periorbital adverse events
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Assessment method [3]
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Timepoint [3]
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Primary outcome [4]
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occurrence of serious adverse events.
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Assessment method [4]
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Timepoint [4]
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Eligibility
Key inclusion criteria
* Patients with open angle glaucoma and/or ocular hypertension requiring a reduction of IOP who were insufficiently responsive to topical betablockers
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Minimum age
18
Years
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Maximum age
No limit
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Sex
Both males and females
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Can healthy volunteers participate?
No
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Key exclusion criteria
* Previous and current treatment with any topical ophthalmic drug containing prostaglandins; any condition in which treatment with the betablocking agent, timolol, was contraindicated.
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Study design
Purpose of the study
Treatment
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Allocation to intervention
Non-randomised trial
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Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
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Masking / blinding
Open (masking not used)
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Who is / are masked / blinded?
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Intervention assignment
Single group
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Other design features
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Phase
Phase 3
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Type of endpoint/s
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Statistical methods / analysis
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Recruitment
Recruitment status
Completed
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Data analysis
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Reason for early stopping/withdrawal
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Other reasons
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Date of first participant enrolment
Anticipated
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Actual
1/02/2002
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Date of last participant enrolment
Anticipated
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Actual
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Date of last data collection
Anticipated
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Actual
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Sample size
Target
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Accrual to date
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Final
976
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Recruitment in Australia
Recruitment state(s)
NSW
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Recruitment hospital [1]
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Pfizer Investigational Site - Sydney
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Recruitment postcode(s) [1]
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2000 - Sydney
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Recruitment postcode(s) [2]
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2067 - Sydney
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Recruitment outside Australia
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Belgium
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Antwerpen
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Belgium
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Brussel
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Belgium
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Edegem
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Belgium
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Gent
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Belgium
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Belgium
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Denmark
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Odense C
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France
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Dijon
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Figeac
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France
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Haguenau
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France
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Le Cannet
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France
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Loos
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France
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Marseille
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France
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Paris
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France
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Versailles
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Germany
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Freising
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Germany
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Germany
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Mainz
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Pisa
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Uppsala
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Birmingham
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Glasgow
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Lancaster
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United Kingdom
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London
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Funding & Sponsors
Primary sponsor type
Commercial sector/industry
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Name
Pfizer
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Address
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Country
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Ethics approval
Ethics application status
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Summary
Brief summary
To estimate the frequency of patients with ocular/periorbital adverse events. To identify any possible long-term adverse consequences of increased iris pigmentation and to follow serious adverse events throughout the study period.
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Trial website
https://clinicaltrials.gov/study/NCT00150267
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Trial related presentations / publications
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Public notes
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Contacts
Principal investigator
Name
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Pfizer CT.gov Call Center
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Address
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Pfizer
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Phone
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Contact person for scientific queries
No information has been provided regarding IPD availability
What supporting documents are/will be available?
No Supporting Document Provided
Results publications and other study-related documents
No documents have been uploaded by study researchers.
Results not provided in
https://clinicaltrials.gov/study/NCT00150267
Download to PDF