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Evaluation of Glycemic Control after Sulfonylurea Withdrawal in Type 2 Diabetic Patients Treated with Combination of Oral Hypoglycemic Agents and Insulin

Evaluation of Glycemic Control after Sulfonylurea Withdrawal in Type 2 Diabetic Patients Treated with Combination of Oral Hypoglycemic Agents and Insulin: A Randomized Controlled Tria

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
TCTR
Registry ID
TCTR20130422001
Enrollment
Unknown
Registered
2013-04-22
Start date
2008-10-16
Completion date
Unknown
Last updated
2026-08-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Type 2 diabetes Insulin&#44

Interventions

comparison between SU withdrawal and SU continuation,withdraw sulfonylurea
Active Comparator Drug,Placebo Comparator Drug
sulfonylurea continuation,SU withdrawal

Sponsors

Routine to Research Unit Siriraj Hospital (R2R)
Lead Sponsor

Eligibility

Sex/Gender
All
Age
30 Years to 75 Years

Inclusion criteria

Inclusion criteria: Type 2 diabetic patients, 30 to 75 year-old, who were treated with insulin in combination with SU, were enrolled in the study. All the subjects have been treated with insulin for at least 3 years and SU at half of the maximum doses or higher. All subjects had hemoglobin A1C levels (HbA1c) of less than 8.5% and stable insulin dosage (less than 10% adjustment) for at least three months prior to the enrollment. Patients who received metformin were included in the study

Exclusion criteria

Exclusion criteria: Patients were excluded if they had other types of diabetes, received treatment with a combination of SU and once-daily insulin, or received thiazolidinediones or other medications which interfered with glucose or lipid metabolism. Other exclusion criteria included history of clinically significant heart disease (New York Heart Association Functional Classification greater than class II or abnormalities other than non-specific ST-T wave changes on the EKG), peripheral vascular disease, pulmonary disease, impaired renal function, poor blood pressure control, electrolyte abnormalities, and neuromuscular diseases.

Design outcomes

Primary

MeasureTime frame
Glycemic control 8 wk HbA1c/ Blood sugar

Secondary

MeasureTime frame
Insulin secretion 2 week Oral glucose tolerance test

Countries

Thailand

Contacts

Public ContactWeerachai Srivanichakorn

Faculty of Medicine Siriraj Hospital, Mahidol University

+66814232161+66814232161

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 9, 2026