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Clinical Trial Summary

The study was a 48-week multicenter, randomized, double-blind, placebo-controlled trial that included 8 weeks of pre-screening and lifestyle education, 32 weeks of treatment, and 16 weeks of follow-up.To observe the efficacy and safety of umbilical cord mesenchymal stem cell infusion in Chinese patients with type 2 diabetic nephropathy who received traditional hypoglycemic therapy.


Clinical Trial Description

The study was a 48-week multicenter, randomized, double-blind, placebo-controlled trial that included 8 weeks of pre-screening and lifestyle education, 32 weeks of treatment, and 16 weeks of follow-up.We plan to recruit 54 subjects,which were divided into experimental group and control group. The volunteers of the experimental group will be given peripheral intravenously a dose of 1.5*10^6/kg human umbilical cord mesenchymal stem cell (HUC-MSC) at 0,8,16,24,32 week. The control group will be given the same dose of saline. Then centralization visit was conducted every 8 weeks until the 48th week.The primary end points include estimated glomerular filtration rate and urinary albumin creatinine ratio(UACR). The secondary end points include HbA1C,plasma insulin and C-peptide, and insulin dose. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04216849
Study type Interventional
Source Shanghai East Hospital
Contact Congrong Wang, MD
Phone +86-021-38804518
Email wcr601@163.com
Status Recruiting
Phase Phase 1/Phase 2
Start date July 1, 2020
Completion date July 1, 2022

See also
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Recruiting NCT05847400 - Predictors of Chronic Kidney Disease Among Type 2 Diabetic Patients in Assiut University Hospitals