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Safety and Exploratory Efficacy Study of UCMSCs in Patients With Fracture and Bone Nonunion

NCT02815423 · Status: UNKNOWN · Phase: PHASE1/PHASE2 · Type: INTERVENTIONAL · Enrollment: 40

Last updated 2016-06-28

No results posted yet for this study

Summary

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.

Conditions

  • Fracture
  • Bone Nonunion

Interventions

BIOLOGICAL

UCMSCs

Transplatation of umbilical cord mesenchymal stem cells

BIOLOGICAL

Percutaneous

Percutaneous injection

Sponsors & Collaborators

  • Guangzhou Panyu Central Hospital

    collaborator OTHER

  • South China Research Center for Stem Cell and Regenerative Medicine

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
60 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2017-01-31
Primary Completion
2019-01-31
Completion
2020-01-31

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02815423 on ClinicalTrials.gov