Table 2 Outcome measures by treatment group.

From: Adjunctive intravenous then oral vitamin C for moderate and severe community-acquired pneumonia in hospitalized adults: feasibility of randomized controlled trial

Clinical outcomes

Vitamin C (n = 36)

Placebo (n = 39)

Total (n = 75)

p value

Died in hospital

0 (0%)

2 (5%)

2 (3%)

0.494

Died within 30 days of treatment initiation

0 (0%)

2 (5%)

2 (3%)

0.494

Died within 90 days of treatment initiation

0 (0%)

4 (10%)

4 (5%)

0.116

Admission to ICU

2 (6%)

4 (11%)

6 (8%)

0.675

Admission to discharge (hours) Median (IQR)

69 (48, 116)

121 (69, 179)

94 (56, 169)

0.071

Treatment to discharge (hours) Median (IQR)

48 (24, 98)

98 (46, 165)

73 (26, 144)

0.098

Treatment to clinical stability (hours) Median (IQR)

22 (-4, 90)

49 (18, 137)

41 (10, 98)

0.083

Plasma vitamin C after 24 h, N (%) (median IQR) a

29 (81%)

226 (131, 461)

32 (82%)

19 (10, 31)

61(81%)

40 (17, 208)

 < 0.0001

Follow-up

 Completed questionnaire N(%)b

31 (86%)

32 (86%)

63 (86.3%)

1

 Readmission within 30 daysb

1 (3%)

(day 24)

4 (11%)

(day 1 & 26)

5 (8%)

0.22

 Readmission for CAPb

1 (2.7%)

1 (2.7%)

2 (2.7%)

1

Further antimicrobial therapy during follow-upc

7 (19%)

5 (14%)

12 (19.0%)

0.52

 No persisting symptomsc

8 (22%)

10 (27%)

18 (29%)

0.64

 Coughc

12 (33%)

10 (27%)

22 (35%)

0.57

 Chest painc

3 (8%)

5 (14%)

8 (13%)

0.51

 Shortness of breathc

14 (39%)

15 (41%)

29 (46%)

0.89

 Returned to normal activitiesc

12 (33%)

13 (35%)

25 (40%)

0.88

 Fatiguec

20 (56%)

14 (38%)

34 (54%)

0.14

  1. Unless otherwise stated values presented are the number of participants (%).
  2. aSamples were not available for vitamin C analysis for day 1 for 7 participants in the vitamin C group, and 7 in the placebo group.
  3. bThe percentage was calculated after excluding those who had died.
  4. cThe percentage was calculated for replies to that question only.