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Pantoprazole on Insulin Secretion in Diabetes (IBP)

Primary Purpose

Type 2 Diabetes

Status
Completed
Phase
Phase 2
Locations
Mexico
Study Type
Interventional
Intervention
Pantoprazole
placebo
Sponsored by
Coordinación de Investigación en Salud, Mexico
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Type 2 Diabetes focused on measuring Diabetes, Insulin, Pantoprazole

Eligibility Criteria

30 Years - 60 Years (Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Type 2 diabetes mellitus
  • Drug-Naive
  • No complications
  • HbA1c 7 to < 9%
  • Fasting plasma glucose < 210mg/dl
  • Body mass index 30.0 to 39.9 and body weight stable for at least 3 months before the study
  • Non smokers
  • Blood pressure < 130/80

Exclusion Criteria:

  • Diabetes complications
  • Women pregnant or stage of lactation
  • Hepatic, renal, autoimmune disease
  • Take drugs with effects on insulin secretion
  • Zollinger-Ellison disease
  • Gastric or pancreatic tumor.

Sites / Locations

  • Instituto Mexicano del Seguro Social. Hospital de Especialidades.

Arms of the Study

Arm 1

Arm 2

Arm Type

Placebo Comparator

Experimental

Arm Label

Placebo

Pantoprazole

Arm Description

Placebo of calcined magnesia, capsules

The pantoprazole will be administered in 40mg capsules

Outcomes

Primary Outcome Measures

First Phase of Insulin Secretion
The hyperglycemic-hyperinsulinemic clamp technique is perform to assess the phases of insulin secretion: first, late and total insulin secretion.
Second Phase of Insulin Secretion
Change from baseline in first phase insulin secretion at 45 day. (plus or minus 3 days)
Total Insulin Secretion
The hyperglycemic-hyperinsulinemic clamp technique is performed to assess the total insulin secretion

Secondary Outcome Measures

Glycated Hemoglobin A1C

Full Information

First Posted
February 20, 2012
Last Updated
January 7, 2014
Sponsor
Coordinación de Investigación en Salud, Mexico
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1. Study Identification

Unique Protocol Identification Number
NCT01541735
Brief Title
Pantoprazole on Insulin Secretion in Diabetes
Acronym
IBP
Official Title
Effect of Pantoprazole on Insulin Secretion in Patients With Type 2 Diabetes
Study Type
Interventional

2. Study Status

Record Verification Date
January 2014
Overall Recruitment Status
Completed
Study Start Date
January 2012 (undefined)
Primary Completion Date
March 2013 (Actual)
Study Completion Date
May 2013 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Coordinación de Investigación en Salud, Mexico

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The purpose of the study is to evaluate the effect of pantoprazole on insulin secretion in drug-naïve patients with type 2 diabetes.
Detailed Description
Type 2 diabetes mellitus (T2DM) has become a major health problem worldwide with a high prevalence and related mortality, and a high rate of disability in the economically active. In Mexico the prevalence was 14.4% reported one of the highest in Latin America and estimated a cost of $ 778 million allocated for this disease in 2010, i.e., the tenth place worldwide. Within its pathophysiology are alterations in the secretion and insulin action, qualitatively and quantitatively, which implies a challenge for long-term metabolic control with the pharmacological arsenal available today. Since the function of pancreatic β cell decreases as a function of time and lack of control is essential metabolic find drugs that can preserve pancreatic cell mass and even promote neogenesis, with the aim of restoring the physiological secretion of insulin have been lost in the early stages of type 2 diabetes to achieve optimal glycemic control sustained over time to avoid complications and reduce the costs associated with the disease. Have been evaluated in animal models with promising results Proton Pumps Inhibitors (PPI) for the restoration of glucose and the preservation of pancreatic cell function, including promoting its growth through increased levels of gastrin, which appears to act as a growth factor. However, at present no such mechanisms have been evaluated in humans, it would be interesting to assess the effect of administration of a PPI such as pantoprazole is, on the phases of insulin secretion in patients with T2DM recent diagnosis. Material and Methods: Randomized, double-blind, placebo controlled clinical trial. Population: 14 drug-naive adults patients with T2DM and obesity. Hyperglycemic-hyperinsulinemic clamp to assess the phases of insulin secretion. Intervention for 45 days: pantoprazole 40mg or placebo.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Type 2 Diabetes
Keywords
Diabetes, Insulin, Pantoprazole

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2, Phase 3
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigator
Allocation
Randomized
Enrollment
14 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
Placebo of calcined magnesia, capsules
Arm Title
Pantoprazole
Arm Type
Experimental
Arm Description
The pantoprazole will be administered in 40mg capsules
Intervention Type
Drug
Intervention Name(s)
Pantoprazole
Other Intervention Name(s)
Pantozol
Intervention Description
The pantoprazole will be administered in capsules of 40mg. The dose will be 1 capsule per day during 45 days.
Intervention Type
Drug
Intervention Name(s)
placebo
Intervention Description
Placebo 40 mg dose.
Primary Outcome Measure Information:
Title
First Phase of Insulin Secretion
Description
The hyperglycemic-hyperinsulinemic clamp technique is perform to assess the phases of insulin secretion: first, late and total insulin secretion.
Time Frame
Change from Baseline at 45 days. (plus or minus 3 days)
Title
Second Phase of Insulin Secretion
Description
Change from baseline in first phase insulin secretion at 45 day. (plus or minus 3 days)
Time Frame
Baseline and 45 day
Title
Total Insulin Secretion
Description
The hyperglycemic-hyperinsulinemic clamp technique is performed to assess the total insulin secretion
Time Frame
Change from baseline of total insulin secretion at 45 day (plus or minus 3 days)
Secondary Outcome Measure Information:
Title
Glycated Hemoglobin A1C
Time Frame
Change from Baseline in glycated hemoglobin A1C at 45 day.

10. Eligibility

Sex
All
Minimum Age & Unit of Time
30 Years
Maximum Age & Unit of Time
60 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Type 2 diabetes mellitus Drug-Naive No complications HbA1c 7 to < 9% Fasting plasma glucose < 210mg/dl Body mass index 30.0 to 39.9 and body weight stable for at least 3 months before the study Non smokers Blood pressure < 130/80 Exclusion Criteria: Diabetes complications Women pregnant or stage of lactation Hepatic, renal, autoimmune disease Take drugs with effects on insulin secretion Zollinger-Ellison disease Gastric or pancreatic tumor.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Manuel Gonzalez, PhD
Organizational Affiliation
Instituto Mexicano del Seguro Social. Centro Medico Nacional de Occidente. Unidad de Investigación Médica en Epidemiologia Clínica
Official's Role
Principal Investigator
Facility Information:
Facility Name
Instituto Mexicano del Seguro Social. Hospital de Especialidades.
City
Guadalajara
State/Province
Jalisco
ZIP/Postal Code
44380
Country
Mexico

12. IPD Sharing Statement

Citations:
PubMed Identifier
25704601
Citation
Gonzalez-Ortiz M, Martinez-Abundis E, Mercado-Sesma AR, Alvarez-Carrillo R. Effect of pantoprazole on insulin secretion in drug-naive patients with type 2 diabetes. Diabetes Res Clin Pract. 2015 Apr;108(1):e11-3. doi: 10.1016/j.diabres.2015.01.039. Epub 2015 Feb 7.
Results Reference
derived

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Pantoprazole on Insulin Secretion in Diabetes

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