Welcome to the Clinical Data Research Hub (CDRH), a coordinating centre for clinical research, hosted by the Liggins Institute and supporting the ON TRACK Network. In collaboration with the Department of Obstetrics and Gynecology, and Department of Paediatrics: Child and Youth Health, University of Auckland.
Contact: researchhub@auckland.ac.nz +6499237713
Databases and randomisation: www.ligginstrials.org
CDRH Guides
- Planning a Trial
- Clinical Trial Terminology
- Study Protocol
- Ethics
- Trial Committees
- Authorship
- Data Sharing
- Māori Responsiveness
- Standard Operating Procedures
Randomisation
Data Management
Analysis
- Normal Distribution Calculator
- OpenEpi - Open Source Statistics
- Medcalc Calculators
- SAS Guides
- NZDep2013 Index of Deprivation
- Trial Analysis
- Data Cleaning
- Diagnostic Tests
Follow-up
- Bayley Scales Age Calculator
- LifePath Follow-up SharePoint
- NZ Travel Calculator
- Definitions for Follow-up Studies
CDRH Admin
- Redmine
- CDRH SharePoint (runs best in IE)
- Liggins VPN Access
- University of Auckland Staff Intranet
- Space statistics
- LiFePATH Admin
- CDRH Randomisation Demo (code:991000tst)
- CDRH Data Environment
Consensus Statements and Checklists
Protocols
Outcomes
- COMET - Core Outcome Measures in Effectiveness Trials
- COS - Prevention of Preterm Birth
- Neonatal Infection Case Definition (Brighton Collaboration)
Reporting
- CONSORT 2010 - Reporting Parallel Group RCTs
- CONSORT 2010 - Extension to Cluster RCTs
- CONSORT 2010 - Extension to Noninferiority / Equivalence RCTs
- StRONNG Checklist - Reporting of Neonatal Nutrition and Growth
- STROBE Statement - Reporting Observational Studies
- STROBE Statement - Explanation & Elaboration
- STARD 2015 - Diagnostic Accuracy Studies
- TIDieR Checklist - Reporting of Interventions
- Very Preterm Birth Studies (Pediatrics 2016)
Analysis
Data & Safety Monitoring
- DAMOCLES - Charter for Clinical Trial Data Monitoring Committees
- ERCIN 2011 - Standards Requirements for GCP-Compliant Data Management in Multinational Clinical Trials
- NAESS 2019 - Neonatal Adverse Event Severity Scale (INC)
Synthesis & Translation
- PRISMA-P 2015 - Preferred Reporting for Systematic Review and Meta-analysis Protocols
- PRISMA 2009 - Preferred Reporting Items for Systematic Reviews and Meta-analyses
- PRISMA-IPD 2015 - Preferred Reporting Items for a Systematic Review and Meta-analysis of Individual Participant Data
- PRISMA Extension 2015 - Network Meta-analyses
- PRISMA-C Extension 2016 - Systematic Reviews and Meta-analyses of Newborn and Child Health Research
- PRISMA-DTA - Preferred Reporting Items for a Systematic Review and Meta-analysis of Diagnostic Test Accuracy Studies
- MOOSE - Reporting of Meta-analysis of Observational Studies in Epidemiology
- GRADE - Grading Quality of Evidence and Strength of Recommendations
- GRADE - Non-Randomised Studies
- AGREE II - Assessing Quality and Reporting of Practice Guidelines
- PROSPERO Registration of Systematic Reviews - Checklist
- ROBINS-I - Risk of Bias In Non-randomized Studies of Interventions
- Risk of Bias Tool for Observational Studies
- Meta-analysis of Animal Studies
- Median to Mean Calculator
- Cochrane Handbook 2019
- WHO Guideline to Rapid Reviews
Laboratory
Training
- NIH Protecting Human Subjects certificate
- NIH GCP course
- ROCHE GCP course (runs best in Firefox)
- Cultural Competency
- Infection control
- Definition of Research and Audit
- Classification of Observational Studies
- Introductory Online Statistics Course
Key Links
ANZ
- Australia & New Zealand Clinical Trials Register (ANZCTR)
- Health and Disability Ethics Committees NZ (HDEC)
- Health Research Council NZ (HRC)
- IMPACT Clinical Trials Network
- MedSafe NZ
- Neonatal Unit Contacts NZ
- Online Forms NZ (HDEC / SCOTT)
- DHB Research Contacts
- Therapeutic Goods Agency (TGA) Australia
- Kidz First Neonatal Research
- Cure Kids Portal
- Ministry of Health NZ