Table 4.
Study Design | Type of ES | Exposure Duration | Experimented on | Key Outcome(s) | Reference |
---|---|---|---|---|---|
RCT | DW | 14 days | 20 healthy subjects, served as own control |
Increase in VEGF, collagen, epidermal cells, and cell apoptotic markers |
[43] |
RCT | DW | 14–20 days | 40 healthy subjects, served as own control |
Reduced wound volume, increased perfusion and vascularity | [44] |
In vitro | Pulsed DC | At 4, 8, and 24 h | Human umbilical vein endothelial cell cultures | Increase in endothelial cell migration and VEGF production | [45] |
In vitro | DC | At 2, 4, and 6 h | Human fibroblast cells in a wound model | Increase in FGF and differentiation of fibroblasts |
[46] |
In vitro | DC | 10 min | Fibronectin coated and non-fibronectin coated dermal fibroblast cells | Increased random migration of fibroblast cells, no increase in dermal fibroblast gene expression | [47] |
In vitro | AC | 12 h | Dermal cell matrix | Dermal fibroblasts entered into the growth phase of cell cycle with continuous ES exposure | [48] |
In vitro | DC and DW | 16 days | Punch biopsies on sample human skin tissues | Increase in epidermis thickness and keratinocyte proliferation | [49] |