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| Name | Class |
|---|---|
| Guangzhou Panyu Central Hospital | OTHER |
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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.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| UCMSCs | Experimental | Transplantation of umbilical cord mesenchymal stem cells (UCMSCs) in patients with fracture and bone nonunion. |
|
| Placebo | Placebo Comparator | The patients with fracture and bone nonunion who underwent percutaneous injection of placebo. |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| UCMSCs | Biological | Transplatation of umbilical cord mesenchymal stem cells |
| |
| Measure | Description | Time Frame |
|---|---|---|
| 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 | 12 months |
| Measure | Description | Time Frame |
|---|---|---|
| Comparison of the rate of complications between the 2 groups | 12 months | |
| Incidence of increased temperature sensitivity by questionnaire | 6 months | |
| Incidence and severity of infections at grafting sites by questionnaire |
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Inclusion Criteria:
Exclusion Criteria:
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| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Xuetao Pei, M.D., Ph.D | Contact | 8610-68164807 | AMMS0906@163.com | |
| Sihan Wang, Ph.D | Contact | 8620-89199011 | wangsihan@scrm.org.cn |
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| ID | Term |
|---|---|
| D050723 | Fractures, Bone |
| ID | Term |
|---|---|
| D014947 | Wounds and Injuries |
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| ID | Term |
|---|---|
| D000279 | Administration, Cutaneous |
| ID | Term |
|---|---|
| D000287 | Administration, Topical |
| D004333 | Drug Administration Routes |
| D004358 | Drug Therapy |
| D013812 | Therapeutics |
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| Percutaneous |
| Biological |
Percutaneous injection |
|
| 6 months |