Table 1.
Analysis | Endpoints | Study criteria | Assessment period |
||
---|---|---|---|---|---|
∼24 weeks | ∼52 weeks | Study end | |||
Primary analysis Full publications | Change from baseline in number of headache days | All studies | ✓ | ✓ | |
Prospective studies* | ✓ | ✓ | |||
Change from baseline in number of days of acute headache pain medication intake | All studies | ✓ | ✓ | ||
Prospective studies* | N/A | N/A | |||
Rate of ≥50% reduction in migraine days | All studies | ✓ | N/A | ||
Prospective studies* | ✓ | N/A | |||
Change from baseline in total HIT-6 score | All studies | ✓ | ✓ | ||
Prospective studies* | N/A | N/A | |||
Change from baseline in MSQ score | All studies | ✓ | ✓ | ||
Prospective studies* | |||||
MIDAS score | All studies | ✓ | N/A | ||
Prospective studies* | ✓ | N/A | |||
Sensitivity analysis 1Full publications | Change from baseline in number of headache days | All studies | ✓ | ||
Prospective studies* | ✓ | ||||
Change from baseline in number of days of acute headache pain medication intake | All studies | ✓ | |||
Prospective studies* | ✓ | ||||
Change from baseline in total HIT-6 score | All studies | ✓ | |||
Prospective studies* | ✓ | ||||
Change from baseline in MSQ score | All studies | ✓ | |||
Prospective studies* | |||||
MIDAS score | All studies | ✓ | |||
Prospective studies* | ✓ | ||||
Sensitivity analysis 2Full publications + congress abstracts/presentations | Change from baseline in number of headache days | All studies | (Same as primary analysis) | ✓ | |
Sensitivity analysis 3Full publications | Change from baseline in number of headache days | All studies: sponsored vs unsponsored | ✓ | – |
*With durations of least 24 weeks; N/A: not applicable,