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Guidelines for Reporting Outcomes in Trial Reports : comparemela.com
Guidelines for Reporting Outcomes in Trial Reports
This report, the Consolidated Standards of Reporting Trials (CONSORT)–Outcomes 2022 extension, is a consensus statement on the standards for reporting outcomes
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Toronto
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London
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United Kingdom
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America
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Pharma Gmb
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Robin Hayeems
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James Webbe
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Eli Lilly
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Petros Pechlivanoglou
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Lisa Stallwood
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Mss Saeed
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Andrea Chiaramida
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Amgen
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Peter Gilgan Centre For Research
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American College Of Rheumatology
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Cundill Centre For Child
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Pfizer
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Astrazeneca
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Health Sciences
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Forest Pharmaceuticals
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Vertex Pharmaceuticals
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Takeda Pharmaceutical Co Ltd
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Drug Administration
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Sickkids Foundation
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School Of Public Health
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Canadian Institutes Of Health Research
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Key Development Phases
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Laboratory Tests Along With Reliability
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Genentech
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Mental Health
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Novartis
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Transparency Of Health Research
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Canadian Cancer Society
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Research Manitoba
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Td Bank Financial Group
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Imperial College London
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Centre For Addiction
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Children Hospital Research Institute Of Manitoba
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Bristol Myers Squibb
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University Of Vermont
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Larner College Of Medicine
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Regeneron Pharmaceuticals
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Reformulary Group
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Savient Pharmaceuticals
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Division Of Neonatal
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European League
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Health Research
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Consolidated Standards
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Reporting Trials
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Cochrane Methodology Register
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Reporting Planned Endpoints
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Clinical Trials
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Standard Protocol Items
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Interventional Trials
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Development Phases
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Section Ref
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Terms Used
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Checklist Items
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Outcomes Used
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Primary Outcome
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Specific Measurement Variable
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Systolic Blood Pressure
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Analysis Metric
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Change From Baseline
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Final Value
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Time Point
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Each Outcome
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Minimal Important Change
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Outcome Data Were Continuous
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Were Analyzed
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Cutoff Values Used
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Outcome Assessments Were Performed
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Several Time Points After Randomization
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Time Points Used
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Composite Outcome Was Used
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Individual Components
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Composite Outcome
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Outcomes That Were
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Trial Registry
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Trial Protocol
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Study Instruments Used
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Laboratory Tests
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Along With Reliability
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Population Similar
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Study Sample
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Trial Specific Training Necessary
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Study Instruments
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Wechsler Abbreviated Scale
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Processes Used
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Duplicate Measurements
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After Data Collection
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Range Checks
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Outcome Data Values
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Checklist Item
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Sample Size
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Target Difference Between Treatment Groups
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Minimal Important Difference
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Difference Elicitation
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Statistical Methods
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Methods Used
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Secondary Outcomes
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Coprimary Outcomes
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Same Outcome Assessed
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Multiple Time Points
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Subgroup Analyses
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Outcome Data From
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Report That
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Outcome Data Were Excluded
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Assess Patterns
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Handle Missing Outcome Items
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Entire Assessments
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Outcome Analysis Population Relating
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Randomized Analysis
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Prespecified Outcome Analyses
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Estate Where
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Results Can Be Found
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Ancillary Analyses
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There Were
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Analyses That Were
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They Were Performed
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North America
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Peter Gilgan Centre
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Sick Children
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Interest Disclosures
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Cundill Centre
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Youth Depression
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Canadian Institutes
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Hospital Research Institute
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Cochrane Prospective Meta Analysis Methods
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Hoffmann La Roche
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Horizon Therapeutics
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American College
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Treating Anxiety Disorders
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Young Children
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Financial Group
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Drs Butcher
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Executive Deputy Editor
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Cochrane Neonatal
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Neonatal Perinatal Medicine
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Larner College
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Chris Gale
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Neonatal Medicine
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Public Health
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Open Science Framework
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