Perinatal a clinical trials coordinating centre in maternal and perinatal health In collaboration Dr Chris McKinlay +64274725099, c.mckinlay@auckland.
A Set for Evaluation of Interventions to Prevent TIDieR Checklist - Reporting of Interventions metaOpenEpi - open source statistics IMPACT Clinical Trials Australia & New Zealand Clinical Trials Register Global Obstetrics Network Core Outcomes Initiative (COMET) Trial Forge UK Clinical Trials Alliance Australia (ACTACochrane Neonatal Cochrane Pregnancy NIH Clinical Research Toolkit ICH GCP National Maternity Monitoring Group NZ Neonatal Unit Contacts NZMedSafe NZ Liggins Clinical Trials International Prospective Register of Systematic Reviews (PROSPERO)
HUB Guides
Randomisation
Simple
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
- Classification of Observational Studies - Lancet 2002
- Determining Adequate Sample Sizes - Pediatrics 2012
- Factorial RCTs - BMC Medical Research Methodology 2003
- Stepped Wedge RCTs - BMJ 2015
- Accounting for Multiple Births in Neonatal and Perinatal Trials - J Pediatrics 2010
Consensus Statements and Checklists
Protocol DevelopmentFollow-up
- Bayley Scales Age Calculator
- NZ Travel Calculator
- Definitions for Follow-up Studies
- Middlemore Parking and Clinic Bookings
- Middlemore Neonatal Research Parking Instructions
- WHO Child Growth Standards (0-5 years)
- WHO Growth Reference 2007 (5-19 years)
- AAP Pediatric BP Calculator
- Bayley 4
CDRH Admin
- Redmine
- University of Auckland Staff Intranet
- Space statistics
- LiFePATH Admin
- CDRH Randomisation Demo (code:991000tst)
- CDRH Data Environment
Consensus Statements and Checklists
Protocols
Outcomes
Reporting
and Standardised
Outcome - and
& 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
- GRADE Handbook
- Cochrane Handbook 2019 - Systematic Reviews of Interventions
- AGREE II - Assessing Quality and Reporting of Practice Guidelines
- PROSPERO Registration of Systematic Reviews - Checklist
Web Links
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
Key Links
ANZ
