Workshop held Tuesday 17th & Wednesday 18th November 2009 in the Menzies Seminar Room.

The workshop was run by Adrienne Kirby and Merryn Voysey of the NHMRC Clinical Trials Centre. Adrienne and Merryn are both experienced clinical trial statisticians. They have been running workshops on clinical trials and statistical issues as part of a Masters course at University of Sydney for many years.

Click here for Program.

• 1.1 Clinical Trials Overview
• 1.2 Protocol and Consort
• 1.3 Randomisation and Blinding (sources of bias)
• 1.4 Study Management
• 2a.1 Grant Application
• 2a.7 Minimisation
• 3.9 Clinical Trial Design
• 3.10 Ethical Issues
• 3.11 Sample Size
• 3.12 Cllinical Trial Analysis
• 4.13 Non-inferiority and Equivalence
• 4.15 Interim Analyses
• 4.16 JPD Meta analysis
• The Analysis Plan
• The Question

Workshop held Tuesday 17th & Wednesday 18th November 2009 in the Menzies Seminar Room.

The workshop was run by Adrienne Kirby and Merryn Voysey of the NHMRC Clinical Trials Centre. Adrienne and Merryn are both experienced clinical trial statisticians. They have been running workshops on clinical trials and statistical issues as part of a Masters course at University of Sydney for many years.

Click here for Program.

• 1.1 Clinical Trials Overview
• 1.2 Protocol and Consort
• 1.3 Randomisation and Blinding (sources of bias)
• 1.4 Study Management
• 2a.1 Grant Application
• 2a.7 Minimisation
• 3.9 Clinical Trial Design
• 3.10 Ethical Issues
• 3.11 Sample Size
• 3.12 Cllinical Trial Analysis
• 4.13 Non-inferiority and Equivalence
• 4.15 Interim Analyses
• 4.16 JPD Meta analysis
• The Analysis Plan
• The Question