The purpose of the present study is to evaluate the safety and exploratory efficacy of the umbilical cord mesenchymal stem cells for patients with fracture and bone nonunion.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
40
Transplatation of umbilical cord mesenchymal stem cells
Percutaneous injection
Radiological progression of bone fusion
After patients receiving mesenchymal stem cells or placebo, imaging control by X-ray and CT, and then analysis by software(ImageJ ) at 1, 6 and 12 months
Time frame: 12 months
Comparison of the rate of complications between the 2 groups
Time frame: 12 months
Incidence of increased temperature sensitivity by questionnaire
Time frame: 6 months
Incidence and severity of infections at grafting sites by questionnaire
Time frame: 6 months
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