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Trial details imported from ClinicalTrials.gov

For full trial details, please see the original record at https://clinicaltrials.gov/study/NCT02399072




Registration number
NCT02399072
Ethics application status
Date submitted
23/03/2015
Date registered
26/03/2015
Date last updated
9/08/2019

Titles & IDs
Public title
A Study of Disease Progression in Participants With Geographic Atrophy Secondary to Age-Related Macular Degeneration
Scientific title
A Multicenter, Prospective Epidemiologic Study of the Progression of Geographic Atrophy Secondary to Age-Related Macular Degeneration
Secondary ID [1] 0 0
2014-003940-11
Secondary ID [2] 0 0
GX29639
Universal Trial Number (UTN)
Trial acronym
Linked study record

Health condition
Health condition(s) or problem(s) studied:
Geographic Atrophy 0 0
Condition category
Condition code
Eye 0 0 0 0
Diseases / disorders of the eye
Other 0 0 0 0
Research that is not of generic health relevance and not applicable to specific health categories listed above

Intervention/exposure
Study type
Observational
Patient registry
Target follow-up duration
Target follow-up type
Description of intervention(s) / exposure
Other interventions - No intervention

Geographic Atrophy Participants - Participants with unilateral GA or GA in one eye and choroidal neovascularization (CNV; active or treated) with or without GA, in the contralateral eye, will be evaluated for the progression of GA for up to approximately 60 months.


Other interventions: No intervention
No intervention administered in this study
Intervention code [1] 0 0
Other interventions
Comparator / control treatment
Control group

Outcomes
Primary outcome [1] 0 0
Mean Change from Baseline in the GA Area as Assessed by Fundus Autofluorescence (FAF) up to Month 60
Timepoint [1] 0 0
Baseline up to Month 60
Secondary outcome [1] 0 0
Change from Baseline in Best Corrected Visual Acuity (BCVA) Score as Assessed by Early Treatment Diabetic Retinopathy Study (ETDRS) Chart up to Month 60
Timepoint [1] 0 0
Baseline up to Month 60
Secondary outcome [2] 0 0
Change from Baseline in BCVA Score as Assessed by ETDRS Chart Under Low Luminance Conditions up to Month 60
Timepoint [2] 0 0
Baseline up to Month 60
Secondary outcome [3] 0 0
Change from Baseline in Binocular Reading Speed as Assessed by Minnesota Low-Vision Reading Test (MNRead) Cards or Radner Reading Cards up to Month 60
Timepoint [3] 0 0
Baseline up to Month 60
Secondary outcome [4] 0 0
Change from Baseline in Monocular Reading Speed as Assessed by MNRead Cards or Radner Reading Cards up to Month 60
Timepoint [4] 0 0
Baseline up to Month 60
Secondary outcome [5] 0 0
Change from Baseline in Binocular Critical Print Size as Assessed by MNRead Cards or Radner Reading Cards up to Month 60
Timepoint [5] 0 0
Baseline up to Month 60
Secondary outcome [6] 0 0
Change from Baseline in Monocular Critical Print Size as Assessed by MNRead Cards or Radner Reading Cards up to Month 60
Timepoint [6] 0 0
Baseline up to Month 60
Secondary outcome [7] 0 0
Change from Baseline in Near Activity Subscale as Assessed by National Eye Institute Visual Functioning Questionnaire 25-Item Version (NEI VFQ-25) up to Month 60
Timepoint [7] 0 0
Baseline up to Month 60
Secondary outcome [8] 0 0
Change from Baseline in Distance Activity Subscale as Assessed by NEI VFQ-25 up to Month 60
Timepoint [8] 0 0
Baseline up to Month 60
Secondary outcome [9] 0 0
Change from Baseline in Composite Scores as Assessed by NEI VFQ-25 up to Month 60
Timepoint [9] 0 0
Baseline up to Month 60
Secondary outcome [10] 0 0
Change from Baseline in Functional Reading Independence Score up to Month 60
Timepoint [10] 0 0
Baseline up to Month 60
Secondary outcome [11] 0 0
Percentage of Participants With Medical Events
Timepoint [11] 0 0
Baseline up to Month 60
Secondary outcome [12] 0 0
Percentage of Participants With Ocular Events
Timepoint [12] 0 0
Baseline up to Month 60

Eligibility
Key inclusion criteria
* Well-demarcated area of GA secondary to AMD
* Women of childbearing potential and men must agree to use adequate contraception for at least 30 days after fluorescein dye administration
* The study is recruiting participants in two different cohorts:

Cohort 1: Participants with unilateral GA OR Cohort 2: Participants with GA in one eye and CNV (active or treated) with or without GA, in the contralateral eye
Minimum age
50 Years
Maximum age
No limit
Sex
Both males and females
Can healthy volunteers participate?
No
Key exclusion criteria
* Previous participation in any studies of investigational drugs for GA / dry AMD (exception for studies of vitamins and minerals)
* GA in either eye due to causes other than AMD
* History of vitrectomy surgery, submacular surgery, or any surgical intervention for AMD
* Previous laser photocoagulation for CNV, diabetic macular edema, retinal vein occlusion, and/or proliferative diabetic retinopathy
* Any ocular/systemic medical conditions that, in the opinion of the investigator, could contribute to participant's inability to participate in the study or interfere with study assessments.
* Requirement for continuous use of therapy indicated in Prohibited Therapy

Study design
Purpose
Duration
Selection
Timing
Statistical methods / analysis

Recruitment
Recruitment status
Stopped early
Data analysis
Reason for early stopping/withdrawal
Other reasons
Date of first participant enrolment
Anticipated
Actual
30/03/2015
Date of last participant enrolment
Anticipated
Actual
Date of last data collection
Anticipated
Actual
8/02/2018
Sample size
Target
Accrual to date
Final
202
Recruitment in Australia
Recruitment state(s)
NSW,SA,VIC,WA
Recruitment hospital [1] 0 0
Marsden Eye Research Centre - Parramatta
Recruitment hospital [2] 0 0
Adelaide Eye and Retina Centre - Adelaide
Recruitment hospital [3] 0 0
Royal Victorian Eye and Ear Hospital - East Melbourne
Recruitment hospital [4] 0 0
The Lions Eye Institute - Nedlands
Recruitment postcode(s) [1] 0 0
2150 - Parramatta
Recruitment postcode(s) [2] 0 0
5000 - Adelaide
Recruitment postcode(s) [3] 0 0
3002 - East Melbourne
Recruitment postcode(s) [4] 0 0
6009 - Nedlands
Recruitment outside Australia
Country [1] 0 0
United States of America
State/province [1] 0 0
Florida
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United States of America
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Missouri
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United States of America
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North Carolina
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United States of America
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Ohio
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United States of America
State/province [5] 0 0
South Carolina
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United States of America
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Tennessee
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United States of America
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Texas
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United States of America
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West Virginia
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Argentina
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Buenos Aires
Country [10] 0 0
Argentina
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Capital Federal
Country [11] 0 0
Argentina
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Cordoba
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Argentina
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Mendoza
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Brazil
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SP
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Canada
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British Columbia
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Canada
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Nova Scotia
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Canada
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Ontario
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Canada
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Quebec
Country [18] 0 0
France
State/province [18] 0 0
Creteil
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France
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Dijon
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France
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Lyon cedex
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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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Poitiers
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France
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St Cyr Sur Loire
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Germany
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Bonn
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Germany
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Köln
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Germany
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Münster
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Germany
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Regensburg
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Hungary
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Budapest
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Hungary
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Debrecem
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Hungary
State/province [31] 0 0
Pecs
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Italy
State/province [32] 0 0
Lazio
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Italy
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Lombardia
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Poland
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Bydgoszcz
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Bytom
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Gdansk
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Katowice
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Krakow
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Wroclaw
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Lódz
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Spain
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Barcelona
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Spain
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Navarra
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United Kingdom
State/province [43] 0 0
Bradford
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United Kingdom
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Bristol
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United Kingdom
State/province [45] 0 0
London
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United Kingdom
State/province [46] 0 0
Southhampton

Funding & Sponsors
Primary sponsor type
Commercial sector/industry
Name
Hoffmann-La Roche
Address
Country

Ethics approval
Ethics application status

Summary
Brief summary
Trial website
Trial related presentations / publications
Public notes

Contacts
Principal investigator
Name 0 0
Clinical Trials
Address 0 0
Hoffmann-La Roche
Country 0 0
Phone 0 0
Fax 0 0
Email 0 0
Contact person for public queries
Name 0 0
Address 0 0
Country 0 0
Phone 0 0
Fax 0 0
Email 0 0
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/NCT02399072