Efficacy and Safety of Empagliflozin in NODAT

Sponsor
RenJi Hospital (Other)
Overall Status
Unknown status
CT.gov ID
NCT03642184
Collaborator
(none)
70
1
2
29.6
2.4

Study Details

Study Description

Brief 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.

Detailed 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.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
70 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Efficacy and Safety of Empagliflozin Compared With Linagliptin in New-onset Diabetes Mellitus After Kidney Transplantation
Actual Study Start Date :
Jul 14, 2018
Anticipated Primary Completion Date :
Dec 31, 2020
Anticipated Study Completion Date :
Dec 31, 2020

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: Empagliflozin

Jardiance 10mg/25mg Film-coated tablets, once daily

Drug: Empagliflozin
Dosage adjustment based on glucose targets . Once daily
Other Names:
  • Jardiance
  • Active Comparator: Linagliptin

    Trajenta 5mg Film-coated tablets, once daily

    Drug: Linagliptin
    Dosage adjustment based on glucose targets. Once daily
    Other Names:
  • Tradjenta
  • Outcome Measures

    Primary Outcome Measures

    1. eGFR [24 weeks]

      the change from baseline in estimated glomerular filtration rate calculated by MDRD formula

    Secondary Outcome Measures

    1. Graft loss rate [24 weeks]

      the frequency of patients' graft loss or dysfunction

    2. Mortality rate [24 weeks]

      the patients' death rate related to treatment and transplantation with in 24 weeks after treatment

    3. Acute rejection [24 weeks]

      the frequency of acute rejection

    4. Progression to albuminuria [24 weeks]

      the frequency of macroalbuminuria

    5. Progression to macroalbuminuria [24 weeks]

      the frequency of macroalbuminuria

    6. Fasting plasma glucose [24 weeks]

      Change from baseline in fasting plasma glucose

    7. Glycated hemoglobin (HbA1c) [24 weeks]

      Change from baseline in HbA1c

    8. Adverse events [24 weeks]

      Record adverse events that related to treatment and transplantation

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years to 65 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    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

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Department of nephrology, endocrinology and kidney transplantation , Ren Ji Hospital, Shanghai Jiao Tong University School of Medicine Shanghai Shanghai China 200127

    Sponsors and Collaborators

    • RenJi Hospital

    Investigators

    • Study Chair: Zhaohui Ni, Dr., Renji Hospital, School of Medicine, Shanghai Jiao Tong University
    • Study Director: Shan Mou, Dr., Renji Hospital, School of Medicine, Shanghai Jiao Tong University
    • Principal Investigator: Yaomin Hu, Dr., Renji Hospital, School of Medicine, Shanghai Jiao Tong University
    • Principal Investigator: Ming Zhang, Dr., Renji Hospital, School of Medicine, Shanghai Jiao Tong University

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    RenJi Hospital
    ClinicalTrials.gov Identifier:
    NCT03642184
    Other Study ID Numbers:
    • RJ20180601NODAT
    First Posted:
    Aug 22, 2018
    Last Update Posted:
    Aug 22, 2018
    Last Verified:
    Aug 1, 2018
    Studies a U.S. FDA-regulated Drug Product:
    Yes
    Studies a U.S. FDA-regulated Device Product:
    No
    Product Manufactured in and Exported from the U.S.:
    Yes
    Keywords provided by RenJi Hospital
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Aug 22, 2018