Skip to main content
. 2023 Jan 25;14:1109966. doi: 10.3389/fphar.2023.1109966

TABLE 4.

Comparing clinical changes between the intervention and control groups.

Symptoms (frequency per day) Pomegranate (n = 32) Placebo (n = 32) p-value a
Daily breath shortness
 Baseline 2.00 (0.00–3.00) 1.00 (0.00–2.00) 0.198
 Endpoint (8 weeks) 0.00 (0.00–0.00) 1.00 (0.00–2.00) 0.001
 Changes −1.00 (−3.00) to (0.00) 0.00 (−1.00) to (1.00) <0.001
p-value** <0.001 0.791
 Nocturnal breath shortness
 Baseline 0.00 (0.00–1.00) 0.00 (0.00–1.75) 0.921
 Endpoint (8 weeks) 0.00 (0.00–0.00) 0.00 (0.00–2.00) 0.003
 Changes 0.00 (−1.00) to (0.00) 0.00 (0.00) to (0.00) 0.034
p-value** 0.002 0.821
 Nocturnal waking up Baseline 0.00 (0.00–1.00) 0.00 (0.00–0.75) 0.400
 Endpoint (8 weeks) 0.00 (0.00–0.00) 0.00 (0.00–0.00) 0.188
 Changes 0.00 (−1.00) to (0.00) 0.00 (0.00) to (0.00) 0.028
p-value** 0.002 0.834
 Limitation of asthma-related activity symptoms
 Baseline 0.00 (0.00–1.00) 0.50 (0.00–2.00) 0.222
 Endpoint (8 weeks) 0.00 (0.00–0.00) 0.00 (0.00–2.75) 0.003
 Changes 0.00 (−1.00) to (0.00) 0.00 (0.00) to (0.00) 0.032
p-value** 0.003 0.991
 Consumption of salbutamol spray
 Baseline 0.00 (0.00–0.00) 0.00 (0.00–0.00) 0.601
 Endpoint (8 weeks) 0.00 (0.00–0.00) 0.00 (0.00–0.00) 0.536
 Changes 0.00 (0.00) to (0.00) 0.00 (0.00) to (0.00) 0.222
p-value** 0.172 0.280
a

Mann–Whitney U test ** Wilcoxon test. Values have been expressed as median (25th, 75th percentiles).