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Search / Trial NCT01195090

Adding Sitagliptin or Pioglitazone to Type 2 Diabetes Mellitus Insufficiently Controlled With Metformin and Sulfonylurea

Launched by SUNG-CHEN LIU · Sep 2, 2010

Trial Information

Current as of June 15, 2025

Completed

Keywords

Sitagliptin Pioglitazone Type 2 Diabetes

ClinConnect Summary

This is a prospective, open-label, randomized, parallel, 24-week study. Inclusion criteria: type 2 diabetes patients who were treated with stable doses of sulfonylurea and metformin to their half maximally dose (sulfonylureas \> half maximal dose, and metformin \> 1500 mg/d) for \> 10 weeks. \> 20 years old; A1C:\> 7.0 % and \< 11% Exclusion criteria: insulin use within 12 weeks of the screening visit, any contraindications for use of sitagliptin or pioglitazone, impaired renal function (serum creatinine \> 1.4 mg/dl), alanine aminotransferase (ALT) or aspartate aminotransferase levels (AST...

Gender

ALL

Eligibility criteria

  • Inclusion Criteria:
  • Type 2 diabetes patients who were treated with stable doses of sulfonylurea and metformin to their half maximally dose (sulfonylureas \> half maximal dose, and metformin \> 1500 mg/d) for \> 10 weeks
  • \> 20 years old
  • A1C: \> 7.0 % and \< 11%
  • Exclusion Criteria:
  • Insulin use within 12 weeks of the screening visit
  • Any contraindications for use of sitagliptin or pioglitazone, impaired renal function (serum creatinine \> 1.4 mg/dl), alanine aminotransferase or aspartate aminotransferase levels \> 2.5 times the upper limit of normal
  • Current or prepare to pregnancy and lactation

About Sung Chen Liu

Sung-Chen Liu is a dedicated clinical trial sponsor committed to advancing medical research and improving patient outcomes through innovative study designs and rigorous trial management. With a focus on therapeutic areas such as oncology, neurology, and cardiovascular health, Liu leverages a wealth of expertise in clinical operations and regulatory compliance to ensure the highest standards of safety and efficacy in research. By fostering collaboration among stakeholders and promoting ethical practices, Sung-Chen Liu aims to drive the development of groundbreaking therapies that address unmet medical needs and enhance the quality of life for patients worldwide.

Locations

Taipei, , Taiwan

Patients applied

0 patients applied

Trial Officials

Sung-Chen Liu, MD

Principal Investigator

Division of Endocrinology and Metabolism, Department of Internal Medicine, Mackay Memorial Hospital

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported

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