Table 2.
EEC primary outcome.
Exposures | Nasal response | Results H2–H4 | Results H0–H4 |
---|---|---|---|
Birch allergen (V5) | Negative | 12/30 (40.0%) | 9/30 (30.0%) |
Positive | 18/30 (60.0%) | 21/30 (70.0%) | |
Placebo (V3) | Negative | 30/30 (100.0%) | 30/30 (100.0%) |
The frequency of nasal responses with placebo (V3) versus birch allergen (V5), were statistically significant (p < .0001). During the H2–H4 time period, no participants reported nasal response with placebo (V3), while 18 participants (60%) experienced a rhinitis response to allergen (V5). Similar results were found for the H0–H4 time period, with rhinitis responses in 21 patients (70%) exposed to allergen versus 0 with placebo