Pantoprazole on Insulin Secretion in Diabetes (IBP)
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| ClinicalTrials.gov Identifier: NCT01541735 |
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Recruitment Status :
Completed
First Posted : March 1, 2012
Results First Posted : February 21, 2014
Last Update Posted : February 21, 2014
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| Condition or disease | Intervention/treatment | Phase |
|---|---|---|
| Type 2 Diabetes | Drug: Pantoprazole Drug: placebo | Phase 2 Phase 3 |
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.
| Study Type : | Interventional (Clinical Trial) |
| Actual Enrollment : | 14 participants |
| Allocation: | Randomized |
| Intervention Model: | Parallel Assignment |
| Masking: | Double (Participant, Investigator) |
| Primary Purpose: | Treatment |
| Official Title: | Effect of Pantoprazole on Insulin Secretion in Patients With Type 2 Diabetes |
| Study Start Date : | January 2012 |
| Actual Primary Completion Date : | March 2013 |
| Actual Study Completion Date : | May 2013 |
| Arm | Intervention/treatment |
|---|---|
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Placebo Comparator: Placebo
Placebo of calcined magnesia, capsules
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Drug: placebo
Placebo 40 mg dose. |
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Experimental: Pantoprazole
The pantoprazole will be administered in 40mg capsules
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Drug: Pantoprazole
The pantoprazole will be administered in capsules of 40mg. The dose will be 1 capsule per day during 45 days.
Other Name: Pantozol |
- First Phase of Insulin Secretion [ Time Frame: Change from Baseline at 45 days. (plus or minus 3 days) ]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 [ Time Frame: Baseline and 45 day ]Change from baseline in first phase insulin secretion at 45 day. (plus or minus 3 days)
- Total Insulin Secretion [ Time Frame: Change from baseline of total insulin secretion at 45 day (plus or minus 3 days) ]The hyperglycemic-hyperinsulinemic clamp technique is performed to assess the total insulin secretion
- Glycated Hemoglobin A1C [ Time Frame: Change from Baseline in glycated hemoglobin A1C at 45 day. ]
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| Ages Eligible for Study: | 30 Years to 60 Years (Adult) |
| Sexes Eligible for Study: | All |
| Accepts Healthy Volunteers: | No |
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.
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01541735
| Mexico | |
| Instituto Mexicano del Seguro Social. Hospital de Especialidades. | |
| Guadalajara, Jalisco, Mexico, 44380 | |
| Principal Investigator: | Manuel Gonzalez, PhD | Instituto Mexicano del Seguro Social. Centro Medico Nacional de Occidente. Unidad de Investigación Médica en Epidemiologia Clínica |
| Responsible Party: | Manuel Gonzalez Ortiz, Principal Investigator, Coordinación de Investigación en Salud, Mexico |
| ClinicalTrials.gov Identifier: | NCT01541735 |
| Other Study ID Numbers: |
IBP1301-93 |
| First Posted: | March 1, 2012 Key Record Dates |
| Results First Posted: | February 21, 2014 |
| Last Update Posted: | February 21, 2014 |
| Last Verified: | January 2014 |
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Diabetes Insulin Pantoprazole |
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Diabetes Mellitus Diabetes Mellitus, Type 2 Glucose Metabolism Disorders Metabolic Diseases Endocrine System Diseases Pantoprazole |
Anti-Ulcer Agents Gastrointestinal Agents Proton Pump Inhibitors Enzyme Inhibitors Molecular Mechanisms of Pharmacological Action |

