Linagliptin in Post-renal Transplantation

Sponsor
Universidad de Guanajuato (Other)
Overall Status
Completed
CT.gov ID
NCT03970668
Collaborator
Hospital Regional de Alta Especialidad del Bajio (Other)
28
39.9

Study Details

Study Description

Brief Summary

Post-renal transplanted patients frequently present hyperglycemia immediately after the procedure.

This was a retrospective comparative study performed in post-renal transplanted patients in a single high speciality center with the goal of compare the effect of linagliptin + insulin in post-renal transplanted patients with hyperglycemia Interventions were linagliptin 5mg daily plus insulin vs insulin alone during 5 days after renal transplantation with hyperglycemia, and the main outcome were glucose levels, insulin dose and severity of hypoglycemia

Condition or Disease Intervention/Treatment Phase

Detailed Description

This was a retrospective comparative study performed in a single center between 2016 and 2018, included the data collected from 28 hospitalized post-renal transplanted patients that presented hyperglycemia (>140 mg/dl or or 7.77 mmol/l) immediately after renal transplantation (RT); 14 patients were treated with linagliptin 5mg daily plus a basal bolus insulin scheme prescribed by the Endocrinology group at the hospital, and 14 patients treated only with basal bolus insulin scheme were randomly selected from a list of patients treated during the same period of time and by the same Endocrinology group. Linagliptin dose was 5mg daily and the basal bolus insulin regimen was started and adjusted according to the international guidelines; in general, patients received a starting insulin dose of around 0.5 U/kg/day, given half as basal insulin (NPH or Glargine) once or twice daily and half as insulin lispro divided into three equal doses before meals. Insulin dose was adjusted daily to achieve the goal of fasting glucose between 80-140 mg/dl (4.44-7.77 mmol/l) or random glucose levels below 180 mg/dl (9.99 mmol/l). Correctional insulin dose was used before each meal, depending on the glucose measurements, starting at 1 unit for each 40mg above 140 mg/dl (7.77 mmol/l) of glucose. Glucose levels were monitored at fasting and before each meal, as well as at bedtime according to standard clinical practice. Data regarding fasting and preprandial glucose levels, hypoglycemia, renal function, and immunosuppression therapy were recorded from the patient´s file during the first 5 days after RT; fasting glucose and renal function were also recorded at 1, 6 and 12 months after RT. Patients were included if they were between 18-65 years of age and presented fasting hyperglycemia (>140 mg/dl or 7.77 mmol/l) immediately after RT.

Ethical and Research committee (CEI) at the Hospital approved the study protocol with the number CEI-49-18.

Study Design

Study Type:
Observational
Actual Enrollment :
28 participants
Observational Model:
Cohort
Time Perspective:
Retrospective
Official Title:
Linagliptin Plus Insulin for Hyperglycemia Immediately After Renal Transplantation: A Comparative Study
Actual Study Start Date :
Jan 1, 2016
Actual Primary Completion Date :
Dec 31, 2018
Actual Study Completion Date :
Apr 30, 2019

Arms and Interventions

Arm Intervention/Treatment
Linagliptin plus insulin

Patients that presented hyperglycemia immediately after renal transplantation and received treatment with linagliptin plus insulin

Drug: Linagliptin 5 mg Oral Tablet
Patients received linagliptin 5mg once daily orally plus a basal bolus insulin scheme, if they presented hyperglycemia (glucose levels above than 140 mg/dl)
Other Names:
  • Linagliptin 5mg once daily plus insulin scheme
  • Insulin

    Patients that presented hyperglycemia immediately after renal transplantation and received treatment only with insulin

    Drug: Insulin
    Patients received a basal bolus insulin scheme, if they presented hyperglycemia (glucose levels above than 140 mg/dl)
    Other Names:
  • Basal bolus insulin scheme
  • Outcome Measures

    Primary Outcome Measures

    1. Fasting glucose [5 days]

      Fasting glucose levels at day 5

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years to 65 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • Hyperglycemia (glucose levels above 140 mg/dl) immediately after renal transplantation
    Exclusion Criteria:
    • Incomplete records on the patients file

    • Acute complications such as liver failure

    Contacts and Locations

    Locations

    No locations specified.

    Sponsors and Collaborators

    • Universidad de Guanajuato
    • Hospital Regional de Alta Especialidad del Bajio

    Investigators

    • Principal Investigator: Rodolfo Guardado, MD, Hospital Regional de Alta Especialidad del Bajio

    Study Documents (Full-Text)

    More Information

    Publications

    None provided.
    Responsible Party:
    Rodolfo Guardado Mendoza, Principal Investigator, Universidad de Guanajuato
    ClinicalTrials.gov Identifier:
    NCT03970668
    Other Study ID Numbers:
    • CEI-49-18
    First Posted:
    May 31, 2019
    Last Update Posted:
    Jun 4, 2019
    Last Verified:
    May 1, 2019
    Individual Participant Data (IPD) Sharing Statement:
    Undecided
    Plan to Share IPD:
    Undecided
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Product Manufactured in and Exported from the U.S.:
    No
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Jun 4, 2019