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. 2011 Oct;18(10):1719–1727. doi: 10.1128/CVI.05194-11

Table 2.

Clinical outcomes for subjects in cohort 1a

Outcome Group A (n = 5) Group B (n = 4) Group C (n = 5) Group D (n = 5)
No. with diarrhea (%) 5 (100) 4 (100) 4 (80) 4 (80)
No. with moderate or severe diarrhea (%) 4 (80) 4 (100) 4 (80) 4 (80)
Mean [median] incubation period (hr) (range) 43 [44] (32–51) 42 [43] (35–48) 43 [40] (21–69) 57 [55] (45–71)
Mean [median] diarrhea stool output in 24-hour period (g) (range) 966 [669] (383–2,418) 765 [476] (419–1,687) 1,032 [1,134] (350–1,511) 666 [613] (473–966)
Mean [median] diarrhea total stool output (g) (range) 1,106 [793] (719–2,418) 1,359 [1,051] (448–2,886) 1,707 [1,709] (1,271–2,138) 1,021 [932] (749–1,472)
Mean [median] duration of diarrhea (hr) (range) 36 [37] (12–61) 57 [59] (4–107) 86 [88] (23–143) 52 [55] (28–71)
Mean [median] of the maximum no. of stools in 24 h (range) 9 [6] (3–19) 6 [6] (3–9) 6 [6] (4–7) 5 [5] (3–7)
No. of subjects with fever 1 2 1 0
No. of subjects with vomiting (maximum no. of vomiting episodes) 1 (4) 1 (4) 1 (5) 3 (5)
a

Group A, 2 × 108 CFU with bicarbonate; group B, 2 × 108 CFU with CeraVacx; group C, 2 × 107 CFU with bicarbonate; group D, 2 × 107 CFU with CeraVacx.