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Clinical Trial Details — Status: Terminated

Administrative data

NCT number NCT03642184
Other study ID # RJ20180601NODAT
Secondary ID
Status Terminated
Phase Phase 4
First received
Last updated
Start date July 14, 2018
Est. completion date January 31, 2019

Study information

Verified date November 2023
Source RenJi Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This is an open label, randomized controlled study. We'd like to access the safety and effects of empagliflozin compared with linagliptin in new-onset diabetes after kidney transplantation patients. Our primary endpoints are kidney related indicators and secondary endpoints are glucose and lipid metabolism related indicators and adverse events. We are going to recruit 35 patients for each group and follow six months.


Description:

In recent years, with the development of transplantation technology and immunosuppressive agents, kidney transplantation has made considerable progress. However, for metabolic disorders after kidney transplantation, such as new diabetes after kidney transplantation, there is still insufficient awareness. Since 1964, Starlz et al. first discovered and proposed New-onset diabetes after kidney transplantation(NODAT) in patients after renal transplantation. Scholars from all countries have paid considerable attention to it. The Chinese guidelines indicate that NODAT can increase the risk of graft-related complications, such as rejection, graft loss and infection, and ultimately affect the long-term survival of the recipient. In addition, NODAT has also been shown to increase the risk of cardiovascular events, and cardiovascular disease is associated with more than half of kidney transplant deaths. A retrospective study of 567 renal transplant recipients in China showed that the incidence of NODAT was 24.2%. It can be seen that the incidence of new-onset diabetes after renal transplantation is high and has long-term adverse effects on transplant patients. Therefore, there is an urgent need to evaluate and investigate NODAT's therapeutic drug regimens. According to the study, empagliflozin has a protective effect on the kidney and cardiovascular system, but it has not yet been written into the treatment guidelines for new-onset diabetes after kidney transplantation. Metformin and linagliptin are frequently used in diabetics after renal transplantation, and linagliptin also have a protective effect on the kidneys. Therefore, this experiment wanted to compare the effects between empagliflozin and linagliptin on kidney protection.


Recruitment information / eligibility

Status Terminated
Enrollment 6
Est. completion date January 31, 2019
Est. primary completion date January 31, 2019
Accepts healthy volunteers No
Gender All
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria: - Single kidney transplantation - Normal glucose tolerance or Pre-Diabetes mellitus before transplantation - According to Oral glucose tolerance test results to make the diagnosis of NODAT - Standard triple immunosuppression therapy - HbA1c=10% - Steady hormone usage - BMI 18.5-30kg/m2 - Patient informed consent Exclusion Criteria: - Diabetes patients before transplantation - Pregnancy pregnancy - Type 1 diabetes after kidney transplantation - Severe liver function impairment (AST/ALT 3 times standard value) - Severely impaired renal function (eGFR<45) - Having uncontrolled diseases - History of cancer in the past 5 years (except basal cell carcinoma) and/or cancer treatment - Participating in another trial involving the study drug with in 30 days - Premenopausal women (1 year before the last menstrual period = informed consent) - Alcohol or drug abuse within 3 months of informed consent, affecting compliance Need other drugs to control NODAT

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Empagliflozin
Dosage adjustment based on glucose targets . Once daily
Linagliptin
Dosage adjustment based on glucose targets. Once daily

Locations

Country Name City State
China Department of nephrology, endocrinology and kidney transplantation , Ren Ji Hospital, Shanghai Jiao Tong University School of Medicine Shanghai Shanghai

Sponsors (1)

Lead Sponsor Collaborator
RenJi Hospital

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary eGFR the change from baseline in estimated glomerular filtration rate calculated by MDRD formula 24 weeks
Secondary Graft loss rate the frequency of patients' graft loss or dysfunction 24 weeks
Secondary Mortality rate the patients' death rate related to treatment and transplantation with in 24 weeks after treatment 24 weeks
Secondary Acute rejection the frequency of acute rejection 24 weeks
Secondary Progression to albuminuria the frequency of macroalbuminuria 24 weeks
Secondary Progression to macroalbuminuria the frequency of macroalbuminuria 24 weeks
Secondary Fasting plasma glucose Change from baseline in fasting plasma glucose 24 weeks
Secondary Glycated hemoglobin (HbA1c) Change from baseline in HbA1c 24 weeks
Secondary Adverse events Record adverse events that related to treatment and transplantation 24 weeks
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