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Trial details imported from ClinicalTrials.gov
For full trial details, please see the original record at
https://clinicaltrials.gov/study/NCT00198497
Registration number
NCT00198497
Ethics application status
Date submitted
13/09/2005
Date registered
20/09/2005
Date last updated
15/03/2013
Titles & IDs
Public title
Safety and Efficacy Study of Vitrase for Clearance of Severe Vitreous Hemorrhage
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Scientific title
Phase III Safety and Efficacy Study of Vitrase (Ovine Hyaluronidase) for Ophthalmic Intravitreal Injection for Clearance of Severe Vitreous Hemorrhage
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Secondary ID [1]
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VIT-03-08961X
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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:
Vitreous Hemorrhage
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Diabetic Retinopathy
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Condition category
Condition code
Metabolic and Endocrine
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Diabetes
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Eye
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Diseases / disorders of the eye
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
Treatment: Drugs - Vitrase
Treatment: Drugs - Vitrase
Experimental: Vitrase - Single Hyaluronidase ophthalmic intravitreal injection
Placebo comparator: Placebo - Single Saline solution intravitreal injection
Treatment: Drugs: Vitrase
Hyaluronidase 55 IU in saline solution
Treatment: Drugs: Vitrase
Hyaluronidase 75 IU in saline solution
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Intervention code [1]
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Treatment: Drugs
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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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Vitreous hemorrhage resolution
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Assessment method [1]
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laser treatment of underlying cause of vitreous hemorrhage, or other surgical treatment, or documented evidence of macula \& at least 180 degrees of vitreous base, that vitreous hemorrhage cause is resolved
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Timepoint [1]
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3 months
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Secondary outcome [1]
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Incidence of adverse events
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Assessment method [1]
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Timepoint [1]
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12 months
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Secondary outcome [2]
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Visual Acuity
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Assessment method [2]
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Timepoint [2]
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3 months, 6 months and 12 months
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Eligibility
Key inclusion criteria
* Severe vitreous hemorrhage that obscures visualization of the fundus on indirect ophthalmoscopy, that has been present >/= 1 month by history or exam
* BCVA is worse than 20/200 at time of screening
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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
* Corneal or lenticular abnormalities that preclude fundus observation
* Ongoing ocular infection, inflammation or history of herpetic corneal lesion
* Current or prior retinal detachment or retinal tears or breaks or intraocular tumor
* More than 1 severe vitreous hemorrhage within 6 months
* Previous vitrectomy for any reason
* Hemorrhage is exclusively pre-retinal, or old & organized
* Prior Vitrase for intravitreal injection in either eye
* No light perception in either eye at any time
* Known contraindications to study medication
* Sickle cell disease
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Study design
Purpose of the study
Treatment
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Allocation to intervention
Randomised controlled 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
Blinded (masking used)
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Who is / are masked / blinded?
The people receiving the treatment/s
The people analysing the results/data
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Intervention assignment
Parallel
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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
1/06/1999
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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
1/06/2003
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Sample size
Target
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Accrual to date
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Final
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Recruitment in Australia
Recruitment state(s)
NSW,QLD,SA,VIC
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Recruitment hospital [1]
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Royal North Shore Hospital - St. Leonards
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Recruitment hospital [2]
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University of Sydney - Sydney
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University of Sydney/Westmead Hospital - Westmead
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Royal Brisbane Hospital - Herston
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Royal Adelaide Hospital - Adelaide
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Royal Victorian Eye and Ear Hospital - East Melbourne
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2088 - St. Leonards
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Recruitment postcode(s) [2]
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2000 - Sydney
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2145 - Westmead
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Recruitment postcode(s) [4]
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4029 - Herston
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Recruitment postcode(s) [5]
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5000 - Adelaide
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Recruitment postcode(s) [6]
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3002 - East Melbourne
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Recruitment outside Australia
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Brazil
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Goias
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Brazil
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Minas Gerais
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Brazil
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PR
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Brazil
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RS
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Brazil
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Budapest
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Szeged
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Coppito
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Italy
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Firenze
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Italy
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Durban
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Alberton
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Pretoria
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Alicante
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Valencia
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Hull
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Newcastle Upon Tyne
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Oxford
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Funding & Sponsors
Primary sponsor type
Commercial sector/industry
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Name
Bausch & Lomb Incorporated
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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
The purpose of this study is to determine if intravitreal injection of Vitrase (ovine hyaluronidase) clears vitreous hemorrhage
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Trial website
https://clinicaltrials.gov/study/NCT00198497
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Trial related presentations / publications
Bhavsar AR, Grillone LR, McNamara TR, Gow JA, Hochberg AM, Pearson RK; Vitrase for Vitreous Hemorrhage Study Groups. Predicting response of vitreous hemorrhage after intravitreous injection of highly purified ovine hyaluronidase (Vitrase) in patients with diabetes. Invest Ophthalmol Vis Sci. 2008 Oct;49(10):4219-25. doi: 10.1167/iovs.07-1602. Epub 2008 Apr 25.
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Public notes
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Contacts
Principal investigator
Name
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Lisa R Grillone, PhD
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Address
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ISTA Pharmaceuticals, Inc.
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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/NCT00198497
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