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Effect of Linagliptin + Metformin vs Metformin Alone in Patients With Prediabetes (PRELLIM)

Primary Purpose

Prediabetic State, Insulin Resistance

Status
Completed
Phase
Phase 4
Locations
Mexico
Study Type
Interventional
Intervention
Linagliptin + metformin
Metformin
Sponsored by
Universidad de Guanajuato
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Prediabetic State focused on measuring prediabetes

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Patients with prediabetes, defined for the existence impaired glucose tolerance (Glucose between 140 and 199 mg/dL at the 2 hours of the Oral Glucose Tolerance test (OGTT) ) with or without impaired fasting glucose (Fasting glucose between 100 and 125 mg/dL)
  • Patients who accept to participate in the study and sign the informed consent letter.

Exclusion Criteria:

  • Patients with diagnosed Type 2 Diabetes Mellitus previously or detected during the OGTT
  • Patients in actual treatment or during the last 3 months with metformin, pioglitazone or another antidiabetic drug, including insulin.
  • Serum creatinine > 1.6 mg/dL
  • Hypertriglyceridemia very high (>500 mg/dL)
  • Pregnant women
  • Altered arterial hypertension (Systolic > 180 mmHg or Diastolic >105 mmHg)
  • Excessive alcohol intake, acute or chronic
  • Medications or medical conditions that affect glucose homeostasis (thiazides, beta blockers, glucocorticoids for systemic use, weight-reducing drugs or anorexigenics, Cushing's syndrome, Thyrotoxicosis.

Sites / Locations

  • Universidad de Guanajuato

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Linagliptin + Metformin plus lifestyle

Metformin plus lifestyle

Arm Description

Patients are randomized to receive for 24 months Linagliptin 2.5mg + metformin 850mg every 12 hours. The start of the dose in this group will be gradual so that at the month of treatment the patient can be with the full doses. Together with this, patients will receive a lifestyle modification program seeking to reduce 5-7% of body weigh and increase physical activity to 90-150min/week.

Patients are randomized to receive for 24 months Metformin 850mg every 12 hours. The start of the dose in this group will be gradual so that at the month of treatment the patient can be with the full doses. Together with this, patients will receive a lifestyle modification program seeking to reduce 5-7% of body weigh and increase physical activity to 90-150min/week.

Outcomes

Primary Outcome Measures

Change from basal fasting and post2h OGTT glucose levels at 12 and 24 months
Fasting and post-2h OGTT glucose values (mg/dl)

Secondary Outcome Measures

Change from basal pancreatic beta cell function at 12 and 24 months
Evaluated with the measurements of glucose and insulin during the oral glucose tolerance test; as well as with the glucose and insulin measurements from the hyperglycemic clamp, as the Disposition index.
Change from basal insulin sensitivity at 12 and 24 months
Insulin sensitivity evaluated during the oral glucose tolerance test by the Matsuda index, and reported as an arbitrary units.
Change from basal Weight at 12 and 24 months
Weight measurement during the study, in kg
Incidence of type 2 diabetes
New reported cases with T2D according the the ADA diagnostic criteria

Full Information

First Posted
December 21, 2016
Last Updated
July 5, 2019
Sponsor
Universidad de Guanajuato
Collaborators
Hospital Regional de Alta Especialidad del Bajio
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1. Study Identification

Unique Protocol Identification Number
NCT03004612
Brief Title
Effect of Linagliptin + Metformin vs Metformin Alone in Patients With Prediabetes
Acronym
PRELLIM
Official Title
Effect of Linagliptin + Metformin vs Metformin Alone on the Role of Pancreatic Islet Function, Insulin Resistance and Markers of Cardiovascular Risk in Patients With Prediabetes: Randomized Clinical Trial
Study Type
Interventional

2. Study Status

Record Verification Date
July 2019
Overall Recruitment Status
Completed
Study Start Date
January 2016 (undefined)
Primary Completion Date
May 2019 (Actual)
Study Completion Date
June 2019 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Universidad de Guanajuato
Collaborators
Hospital Regional de Alta Especialidad del Bajio

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Type 2 diabetes is a worldwide epidemic disease, and preventive strategies are needed to face this health problem. The goal of this clinical trial is to evaluate the effect of linagliptin + metformin vs metformin alone on physiopathological parameters, such as glucose metabolism, insulin resistance, insulin secretion and pancreatic beta cell function in patients with impaired fasting glucose plus impaired glucose tolerance, during 24 months.
Detailed Description
The main goal of this clinical trial is to compare the effect of two different treatments during 24 months: Lifestyle modification program + metformin 850mg twice daily Lifestyle modification program + linagliptin (2.5mg) and metformin (850mg) twice daily on the following parameters, after 24 months of treatment: Glucose metabolism, evaluated by the oral glucose tolerance Insulin resistance, evaluated by the oral glucose tolerance in 100% of the patients and by hyperglycemic clamp in 10 % of the patients Insulin secretion, evaluated by the oral glucose tolerance in 100% of the patients and by hyperglycemic clamp in 10 % of the patients Pancreatic beta cell function, evaluated by the oral glucose tolerance in 100% of the patients and by hyperglycemic clamp in 10 % of the patients Systemic inflammation and cardiovascular risk factors, evaluated by cytokines interlelukin-6 (IL6), C-reactive protein (PCR), and measurement of the intima media thickness by ultrasound. All the patients will have a basal evaluation with an oral glucose tolerance test, lipid profile, body composition, and IMT measurement by ultrasonography; and 10 % will be invited for the hyperglycemic clamp. After the basal evaluation, if the patients result with IMPAIRED GLUCOSE TOLERANCE and have at least 2 risk factors, they will be invited to the intervention phase where they will be randomized to one of the two treatment groups. Patients will have a follow-up visit every month to review the adherence to the lifestyle modification program and to the medication. Every 6 months OGTT will be performed on all the patients, and in a subset of patients hyperglycemic clamp will be performed at 0, 6 and 12 months. After 18 and 24 months, patients will repeat the same evaluation performed as the basal evaluation.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Prediabetic State, Insulin Resistance
Keywords
prediabetes

7. Study Design

Primary Purpose
Prevention
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
144 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Linagliptin + Metformin plus lifestyle
Arm Type
Experimental
Arm Description
Patients are randomized to receive for 24 months Linagliptin 2.5mg + metformin 850mg every 12 hours. The start of the dose in this group will be gradual so that at the month of treatment the patient can be with the full doses. Together with this, patients will receive a lifestyle modification program seeking to reduce 5-7% of body weigh and increase physical activity to 90-150min/week.
Arm Title
Metformin plus lifestyle
Arm Type
Active Comparator
Arm Description
Patients are randomized to receive for 24 months Metformin 850mg every 12 hours. The start of the dose in this group will be gradual so that at the month of treatment the patient can be with the full doses. Together with this, patients will receive a lifestyle modification program seeking to reduce 5-7% of body weigh and increase physical activity to 90-150min/week.
Intervention Type
Combination Product
Intervention Name(s)
Linagliptin + metformin
Other Intervention Name(s)
Tradjenta Duo
Intervention Description
Linagliptin-Metformin 2.5/850mg twice daily plus a lifestyle modification program based on nutritional assesment, physical activity prescription and general counseling
Intervention Type
Drug
Intervention Name(s)
Metformin
Intervention Description
Metformin 850mg twice daily plus a lifestyle modification program based on nutritional assesment, physical activity prescription and general counseling
Primary Outcome Measure Information:
Title
Change from basal fasting and post2h OGTT glucose levels at 12 and 24 months
Description
Fasting and post-2h OGTT glucose values (mg/dl)
Time Frame
12 and 24 months
Secondary Outcome Measure Information:
Title
Change from basal pancreatic beta cell function at 12 and 24 months
Description
Evaluated with the measurements of glucose and insulin during the oral glucose tolerance test; as well as with the glucose and insulin measurements from the hyperglycemic clamp, as the Disposition index.
Time Frame
12 and 24 months
Title
Change from basal insulin sensitivity at 12 and 24 months
Description
Insulin sensitivity evaluated during the oral glucose tolerance test by the Matsuda index, and reported as an arbitrary units.
Time Frame
12 and 24 months
Title
Change from basal Weight at 12 and 24 months
Description
Weight measurement during the study, in kg
Time Frame
12 and 24 months
Title
Incidence of type 2 diabetes
Description
New reported cases with T2D according the the ADA diagnostic criteria
Time Frame
24 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients with prediabetes, defined for the existence impaired glucose tolerance (Glucose between 140 and 199 mg/dL at the 2 hours of the Oral Glucose Tolerance test (OGTT) ) with or without impaired fasting glucose (Fasting glucose between 100 and 125 mg/dL) Patients who accept to participate in the study and sign the informed consent letter. Exclusion Criteria: Patients with diagnosed Type 2 Diabetes Mellitus previously or detected during the OGTT Patients in actual treatment or during the last 3 months with metformin, pioglitazone or another antidiabetic drug, including insulin. Serum creatinine > 1.6 mg/dL Hypertriglyceridemia very high (>500 mg/dL) Pregnant women Altered arterial hypertension (Systolic > 180 mmHg or Diastolic >105 mmHg) Excessive alcohol intake, acute or chronic Medications or medical conditions that affect glucose homeostasis (thiazides, beta blockers, glucocorticoids for systemic use, weight-reducing drugs or anorexigenics, Cushing's syndrome, Thyrotoxicosis.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Rodolfo Guardado-Mendoza, MDPhD
Organizational Affiliation
Universidad de Guanajuato
Official's Role
Principal Investigator
Facility Information:
Facility Name
Universidad de Guanajuato
City
León
State/Province
Guanajuato
ZIP/Postal Code
37670
Country
Mexico

12. IPD Sharing Statement

Plan to Share IPD
No
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Effect of Linagliptin + Metformin vs Metformin Alone in Patients With Prediabetes

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