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Table 3 Summary of adverse event in the control and the hUC-MSC groups

From: Therapeutic evidence of umbilical cord-derived mesenchymal stem cell transplantation for cerebral palsy: a randomized, controlled trial

Group

All (n = 39)

Control (n = 20)

hUC-MSC (n = 19)

P valueA

AE

Number (%)

Number (%)

Onset time post-treatment

Number (%)

Onset time post-treatment

24 h

7 days

30 days

After 30 days

24 h

7 days

30 days

After 30 days

Upper respiratory infection

24 (61.54%)

14 (70.0%)

0

1

3

10

10 (52.6%)

0

2

2

6

0.333

Diarrhea

15 (38.46%)

9 (45.0%)

0

0

2

7

6 (31.6%)

0

0

2

4

0.514

Fever

11 (28.21%)

4 (20.0%)

0

1

1

2

7 (36.8%)

3

0

2

2

0.301

Vomiting

8 (20.51%)

3 (15.0%)

0

0

0

3

5 (26.3%)

0

0

1

4

0.451

Constipation

4 (10.26%)

3 (15.0%)

0

0

1

2

1 (5.3%)

0

0

0

1

0.605

  1. Abbreviations: AE adverse event, hUC-MSC human umbilical cord-derived mesenchymal stem cell
  2. AP value was calculated by Fisher’s exact test on the incidence between groups