C-peptide Concentrations in Type 2 Diabetes Treated With Insulin; is it Time to Revise the Treatment of Type 2 Diabetes

Sponsor
Goztepe Training and Research Hospital (Other)
Overall Status
Completed
CT.gov ID
NCT04005261
Collaborator
(none)
249
1
3.9
63.2

Study Details

Study Description

Brief Summary

C-peptide is used to evaluate beta cell reserves. Patients with type 2 diabetes are treated with insulin for different indications. Other than beta-cell insufficiency and organ failures, insulin treatment is needed for a specified period. The investigators want to evaluate beta cell reserves in patients with type 2 diabetes treated with insulin for at least six months to see if that is the case. The investigators also want to compare the characteristics of these patients according to their beta cell reserves.

Condition or Disease Intervention/Treatment Phase
  • Diagnostic Test: C-peptide concentrations

Detailed Description

In patients with type 2 diabetes, initiation of insulin therapy is indicated in several conditions such as severe insulin resistance, acute metabolic decompensations, surgery, pregnancy, and progression of diabetic complications, and also when glycemic control cannot be achieved with effective lifestyle regulation and non-insulin antidiabetic medications. Some of these indications are transient, and patients should be reassessed to choose the appropriate treatment options. Clinical inertia is one of the new topics expressed in the recent diabetes guidelines. The investigators aimed to investigate the beta cell reserves of the patients with type 2 diabetes who are treated with insulin, to see if they have insufficient insulin secretion and if not, to compare their characteristics.

Study Design

Study Type:
Observational
Actual Enrollment :
249 participants
Observational Model:
Case-Only
Time Perspective:
Prospective
Official Title:
Is it Time to Revise Type 2 Diabetes Treatment: C-peptide Concentrations in Type 2 Diabetes Treated With Insulin
Actual Study Start Date :
Nov 1, 2018
Actual Primary Completion Date :
Feb 1, 2019
Actual Study Completion Date :
Mar 1, 2019

Arms and Interventions

Arm Intervention/Treatment
patients with type 2 diabetes treated with insulin

Patients with type 2 diabetes who have been using insulin for at least six months. They should be older than 18 years The patients should be presented to the Diabetes Outpatient Clinics of Istanbul Medeniyet University Goztepe Training and Research Hospital

Diagnostic Test: C-peptide concentrations
The patients will be grouped by their C-peptide concentrations

Outcome Measures

Primary Outcome Measures

  1. The incidence of adequate, borderline and insufficient beta cell reserves assessed by the fasting C-peptide concentrations [3 months]

    Fasting C-peptide concentrations will be measured in patients with type 2 diabetic patients using insulin as a monotherapy or as part of combination therapy and the patients will be grouped as patients with adequate beta cell reserves, patients with borderline beta cell reserves and patient with insufficient beta cell reserves.

  2. Correlations of fasting C-peptide concentrations with patients characteristics and biochemical findings [3 months]

    Correlations of fasting C-peptide concentrations with patients characteristics and biochemical findings, especially the components of metabolic syndrome.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Patients with type 2 diabetes who had been treated with insulin as a monotherapy or as a component of combination therapy for at least 6 months.
Exclusion Criteria:
  • Diagnosis of other types of diabetes,

  • end-stage renal failure,

  • history of renal transplantation,

  • diabetic acute metabolic decompensation,

  • decompensated heart failure,

  • advanced liver disease,

  • pregnancy,

  • acute or chronic pancreatitis,

  • pancreatic carcinoma,

  • acute infections,

  • use of medications that might affect glucose regulation (e.g. corticosteroids)

Contacts and Locations

Locations

Site City State Country Postal Code
1 IMU Goztepe Education and Research Hospital Istanbul Turkey

Sponsors and Collaborators

  • Goztepe Training and Research Hospital

Investigators

  • Principal Investigator: Ayşe N Erbakan, MD, IMU Doctoral program
  • Study Director: Mehmet Uzunlulu, Prof, IMU Goztepe Education and Research Hospital

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Ayse N Erbakan, Principal Investigator, Goztepe Training and Research Hospital
ClinicalTrials.gov Identifier:
NCT04005261
Other Study ID Numbers:
  • C-peptide2019
First Posted:
Jul 2, 2019
Last Update Posted:
Jul 2, 2019
Last Verified:
Jul 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
Keywords provided by Ayse N Erbakan, Principal Investigator, Goztepe Training and Research Hospital
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jul 2, 2019