Clinical Study

Utilizing Autologous Multipotent Mesenchymal Stromal Cells and -Tricalcium Phosphate Scaffold in Human Bone Defects: A Prospective, Controlled Feasibility Trial

Table 1

(a) Demographics of patients in the trial group. (b) Demographics of patients in the control group.
(a)

Case

1 270813420101II13.50
2 161872633210II19.10
3 159862830101III13.51
4 271602520121III4.90
5 272723220131III11.31
6 168862821101III13.20
7 1671023211101III6.01
8 168802510121II50.00
9270733020121II16.01

(b)

Case

1168943110101II13.51
2268873110110II18.750
3266863310121II15.00
4275542010101II22.50
5270933211312II12.00
6270702721121II24.00
7269833120101II10.51
8275782911101IV16.01
9265733020121II16.01

: gender: 1: male; 2: female; : age at revision (years); : weight (kg); : body mass index (kg/m2); : primary diagnosis: 1: osteoarthritis, 2: hip dysplasia, and 3: osteonecrosis; : number of previous revisions; : revision indication: 1: aseptic loosening, 2: instability of arthroplasty, and 3: suspected septic loosening (negative cultures); : cup revision: 0: none, 1: uncemented cup, 2: uncemented cup + morselized allogeneic bone graft, and 3: cemented cup + Burch Schneider + morselized allogeneic bone graft; : femoral component removed: 0: well-fixed and positioned femoral component not removed, 1: cemented, and 2: cement spacer; : AAOS defect classification: II: cavitary, III: combined segmental and cavitary, IV: malalignment, : size of the defect (cm3); : femoral reinforcement: 0: none and 1 cerclage strips.