Clinic-based secondary outcome variables (all Honevo minus control)
Comparison | N with data | Hodges-Lehman estimate (95% CI) | p Value | |
---|---|---|---|---|
Honevo | Control | |||
IGA-RSS week 2 | 66 | 66 | 0 (−1 to 0) | 0.26 |
IGA-RSS week 8 | 61 | 54 | 0 (−1 to 0) | 0.06 |
IGA-RSS week 2 minus baseline | 66 | 66 | −1 (−1 to 0) | 0.03 |
IGA-RSS week 8 minus baseline | 61 | 54 | −1 (−1 to 0) | 0.005 |
Estimate (95% CI) | p Value | |||
IGA-RSS week 8 adjusted for baseline* | 61 | 54 | −0.6 (−1.1 to −0.2) | 0.003 |
Mean difference (95% CI) | p Value | |||
VAS-CS week 2 | 66 | 66 | 9.1 (3.5 to 14.7) | 0.002 |
VAS-CS week 8 | 61 | 54 | 12.3 (5.7 to 18.9) | <0.001 |
VAS-S week 2 | 66 | 66 | −3.6 (−9.9 to 2.7) | 0.26 |
VAS-S week 2 minus baseline | 66 | 66 | −2.9 (−9.2 to 3.5) | 0.38 |
VAS-S week 8 | 61 | 54 | −4.5 (−11.6 to 2.6) | 0.21 |
VAS-S week 8 minus baseline | 61 | 54 | −11.0 (−18.0 to −3.9) | 0.003 |
IGA-RSS: blinded Investigator Global Assessment of Rosacea Severity Score, based on a seven-point scale (0 ‘clear’ to 6 ‘severe’).
VAS-CS: Participant-rated assessment of change in severity of rosacea based on a 100 mm VAS scale (0 mm ‘much worse’ to 100 mm ‘much improved’).
VAS-S: Participant-rated assessment of severity of rosacea based on a 100 mm VAS scale (0 mm ‘mildest possible’ symptoms and 100 mm ‘worst possible’ symptoms).
Analysis of variance (ANOVA) with baseline reading as a covariate, normality assumptions not well met.
*ANOVA with baseline reading as a co-variate, normality assumptions not well met.