Research study designs Flashcards
Questions asked in each phase of drug development
Phase I: Is the drug safe?
- healthy volunteer
- Pharmacokinetics
- AE
Phase II: dose the drug work?
- pts w/ dz
- efficacy of tx
- appropriate dosing
- AE
Phase III: does the drug work better?
FDA approval
Phase IV: Postmarketing surveillance
-less common AE
Long term effects
Meta-analysis
Combines data from many studies
Increases statistical power
Pooling studies – selection bias creeps in
Quality as good as individual study quality
Case control study
W/dz and w/o dz
Look for exposure risk – assoc
Retrospective
Observational – no intervention
-> Odds Ratio
Odds dz and no dz had exposure: A/C / B/D
Odds dz of exposed vs dz of unexposed: A/B / C/D
Cohort study
Common exposure compared to no exposure as control
Observational
Retro or prospective
-> Relative risk
Risk ratio: A/A+B / C/C+D
Rate of dz in exposure group/rate of dz in unexposed group
How many times greater risk bad outcome happens in exposed group
Cross-sectional study
Population at 1 point in time
Snapshot of large population
Prevalence
Observational
Can’t tell you: Incidence Increase or decrease in prevalence How exposures/outcomes related over time Can’t give causality
Twin concordance study
Rates/traits of dz in identical twins and in fraternal twins to measure heritability
Adoption study
Genetics vs environment factors
Twins raised in separate homes
Controlled
Experimental group receives experimental tx
Control group: placebo or comparison drug that’s well known
Randomized
Random assignment to experimental or control group
Limits bias
Double blinded
Participant and investigator don’t know what they are getting/giving