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. 2022 Mar 10;77:103920. doi: 10.1016/j.ebiom.2022.103920

Table 1.

Completed clinical studies of MSCs in the treatment of patients with ARDS.

Numbers Trial ID Sources of MSCs Phase Numbers of patients Doses and administration routes Primary outcomes Refs.
1 NCT01902082 AD-MSCs 1 12 A single dose of 1 × 106 cells/ kg; IV No adverse events or serious adverse events. The clinical effect at this dose is weak. 71
2 Not reported BM-MSCs Case report 2 A single dose of 2 × 106 cells/ kg; IV Oxygenation and pulmonary compliance were improved. Levels of inflammation markers were reduced. 72
3 Not reported UC-MSCs 1 9 A single dose of 1.0 × 106 cells/kg or 5.0 × 106 cells/kg or 1.0 × 107 cells/kg;IV Tolerated without serious adverse events. 73
4 NCT01775774 BM-MSCs 1 9 A single dose of 1 × 106 cells/kg or 5 × 106 cells/kg or 10 × 106 cells/kg;IV Well tolerated and safe. 74
5 NCT02097641 BM-MSCs 2a 60 A single dose of 10 × 106 cells/kg; IV No MSC-related predefined hemodynamic or respiratory adverse events. 75
6 NCT03042143. UC-MSCs 1 9 A single dose of 1 or 2 or 4 × 108; IV Well tolerated. Adverse events included apyrexia, non-sustained ventricular tachycardia, and deranged liver function. 76

MSCs, mesenchymal stem cells; AD-MSCs, adipose-derived MSCs; BM-MSCs, bone marrow autologous MSCs; UC-MSCs, umbilical cord-derived MSCs; IV, intravenous injection.