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A Pilot Study to Evaluate the Effects of Nateglinide Vs. Glibenclamide on Renal Hemodynamics and Albumin Excretion
This study has been completed.
Sponsored by: Novartis
Information provided by: Novartis
ClinicalTrials.gov Identifier: NCT00238472
  Purpose

This study is not being conducted in the United States. The purpose of the study is to evaluate the effects of nateglinide compared to glibenclamide on renal hemodynamics and albumin excretion.


Condition Intervention Phase
Diabetes Mellitus, Type 2
Drug: nateglinide
Phase IV

MedlinePlus related topics: Diabetes
Drug Information available for: Glyburide A 4166
U.S. FDA Resources
Study Type: Interventional
Study Design: Treatment, Randomized, Open Label, Active Control, Parallel Assignment, Efficacy Study
Official Title: A Pilot Study to Evaluate the Effects of Nateglinide Vs. Glibenclamide on Renal Hemodynamics and Albumin Excretion

Further study details as provided by Novartis:

Primary Outcome Measures:
  • Change from baseline in postprandial glomerular filtration rate at 12 weeks

Secondary Outcome Measures:
  • Change from baseline in fasting morning glomerular filtration rate at 12 weeks
  • Change from baseline in postprandial renal plasma flow at 12 weeks
  • Change from baseline in fasting morning renal plasma flow at 12 weeks
  • Change from baseline in adjusted 2-hour postprandial glucose at 12 weeks
  • Change in insulin AUC (0-240 minutes) at 12 weeks

Estimated Enrollment: 24
Study Start Date: May 2003
  Eligibility

Ages Eligible for Study:   18 Years to 75 Years
Genders Eligible for Study:   Both
Criteria

Inclusion Criteria:

  • Type 2 diabetes diagnosed at least 1 year before inclusion
  • Blood glucose criteria must be met
  • Microalbuminuria criteria must be met

Exclusion Criteria:

  • Pregnant or nursing females or females of childbearing potential not using a medically approved birth control method
  • Blood glucose criteria outside the specified range
  • Microalbuminuria criteria outside the specified range
  • Serious cardiovascular events within the past 6 months
  • Other protocol-defined exclusion criteria may apply
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00238472

Sponsors and Collaborators
Novartis
Investigators
Study Director: Novartis Pharmaceuticals Novartis Pharmaceuticals
  More Information

Study ID Numbers: CDJN608AIT05
Study First Received: October 12, 2005
Last Updated: June 1, 2006
ClinicalTrials.gov Identifier: NCT00238472  
Health Authority: United States: Food and Drug Administration

Keywords provided by Novartis:
Type 2 diabetes
nateglinide

Study placed in the following topic categories:
Glyburide
Metabolic Diseases
Diabetes Mellitus, Type 2
Diabetes Mellitus
Nateglinide
Endocrine System Diseases
Endocrinopathy
Metabolic disorder
Glucose Metabolism Disorders

Additional relevant MeSH terms:
Hypoglycemic Agents
Physiological Effects of Drugs
Pharmacologic Actions

ClinicalTrials.gov processed this record on January 14, 2009