Injury | Enrollment number | Design and phase of study | Type of MSCs | Following duration | Infusion method | Dose of injection | Outcome | NCT number | Reference |
---|---|---|---|---|---|---|---|---|---|
COPD | 9 | Matched-control | Autologous BM-MSCs | – | – | – | Feasible | NCT01306513 | [56] |
COPD | 10 | Phase I, prospective open-label | Autologous BM-MSCs | 3 weeks | Intravenous | 1–2 × 106 cells/kg | Feasible and safe | NCT01306513 | [57] |
COPD | 10 | Phase I, prospective, nonrandomized, patient‐blinded, placebo‐controlled | Allogeneic BM-MCs | 90 days | – | 108 cells/kg | Feasible and safe | NCT01872624 | [58] |
COPD | 4 | Phase I | Autologous BM-MCs | 3 years | Intravenous | 108cells/kg | Feasible and safe | NCT01110252 | [59] |
COPD | 9 | Phase I pilot study | Allogeneic BM-MSCs | 1 year | Intravenous | 2 × 106 cells/kg | Feasible and safe | 12,614,000,731,695 | [60] |
COPD | 62 | Randomized, placebo | Allogeneic BM-MSCs | 2 years | – | – | Feasible | NCT00683722 | [62] |
COPD | 62 | Placebo-controlled, randomized, double-blinded | Allogeneic BM-MSCs | 2 years | Intravenous | 108 cells/kg | Feasible and safe | NCT00683722 | [61] |
COPD | 40 | Matched case–control, phase I/II trial | Allogeneic HUC-MSCs | 1 year | Intravenous | 106 cells/kg | Feasible and safe | NCT04433104 | [78] |
COPD | 20 | Controlled, pilot clinical trial | Allogeneic HUC-MSCs | 6 months | Intravenous | 106 cells/kg | Feasible and safe | ISRCTN70443938 | [79] |
COPD | 20 | Matched-control | AD-MSCs and autologous BM-MCs | – | Intravenous | 108 cells/kg | Feasible and safe | NCT02412332 | [80] |