Systematic Reviews
Copyright ©The Author(s) 2025.
World J Stem Cells. Mar 26, 2025; 17(3): 102067
Published online Mar 26, 2025. doi: 10.4252/wjsc.v17.i3.102067
Table 1 Baseline characteristics of randomized clinical trials with cryopreserved human umbilical cord-derived mesenchymal stem cells for heart disease, n (%)
Ref.He et al[20], 2020, ChinaBartolucci et al[21], 2017, ChileUlus et al[19], 2020, Turkey
Study typeRCTRCTOpen-label RCT
PhaseII/III/II
ConditionMIHFMI
Sample sizeTotal503041
Intervention (% male)35 (71.42)15 (80.0)25 (100)
Control (% male)15 (46.67)15 (93.3)16 (100)
Age (mean ± SD)Intervention61 ± 8.257.33 ± 10.0561.8 ± 10
Control65.2 ± 7.957.20 ± 11.6465.3 ± 6.8
BMI (mean ± SD)Intervention25 ± 3.3529.12 ± 2.8826.5 ± 4.5
Control23.59 ± 2.2829.52 ± 4.0026.6 ± 4.8
Number of smokersIntervention11 (31.43)7 (46.7)21 (84)
Control3 (25.0)4 (26.7)15 (88.2)
HTNIntervention24 (68.57)7 (46.7)15 (60)
Control9 (75.0)8 (53.3)11 (64.7)
DMIntervention12 (34.29)5 (33.3)16 (66.7)
Control8 (66.7)7 (46.7)9 (52.9)
NYHA; I (n), II (n), III (n), IV (n)InterventionIII (4/8), IV (12/8)N/S: 2.03 ± 0.61N/S: 1.9 ± 0.44
ControlIII (7) IV (5)N/S: 1.67 ± 0.49N/S: 2.1 ± 0.37
ComparisonCABG onlyPlaceboCABG only
Follow-up3, 6, and 12 months3, 6, and 12 months1, 3, 6, and 12 months
Assessment modality (yes/no)ECGNoYesYes
EchoNoYesYes
MRIYes (CMR)Yes (CMR)Yes
Cardiac CTNoNoNo
SPECTNoNoYes
Measured outcomesSerious adverse events at 12 months (primary), the efficacy of hUC-MSCs and collagen scaffold assessed according to the CV-CMR–based LVEF and infarct size at 3, 6, and 12 months after treatment, and NYHA (secondary)Safety: Adverse events after IV infusion -/-. Efficacy: Primary, changes in LVEF, LVESV & LVEDV by Echo; LVEF, LVESV, and LVEDV by CMR; NYHA score (secondary)LVEF, LV remodeling, myocardial mass, 6MWD, NYHA score change