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Sulfonylurea therapy added on type 2 diabetes patients with poorly controlled insulin therapy in Juntendo

Sulfonylurea therapy added on type 2 diabetes patients with poorly controlled insulin therapy in Juntendo - START-J

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000006765
Enrollment
90
Registered
2012-01-01
Start date
2012-01-01
Completion date
Unknown
Last updated
2026-06-29

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

Conditions

type 2 diabetes

Interventions

addition of glimepiride in insulin therapy no addition of glimepiride

Sponsors

Juntendo University Graduate Schoolof Medicine.
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1)Type 2 diabetes patients whose glycated hemoglobin level are between 7.0 and 10.0 % 2)glycated hemoglobin level were stable during last three months (-0.5 to 0.5%) 3)subjects who are already performing diet and exercise therapy for 6 months 4)subjects who were prescribed insulin for more than 6 months but not done sulfonylurea. 5)no ristriction on the drugs already prescribed. It is possible to add any drug other than sulfonylurea and change dose to avoid adverse effects like hypoglycemia according to the dicision of physician in attendance. 6)subjects who chan understand informed consent

Exclusion criteria

Exclusion criteria: 1) type 1 diabetes 2) patients who have serious liver disease (AST and/or ALT are more than 100IU/L) 3) patients who have serious kidney disease (Serum Cr is more than 2.0mg/dL) 4) patients who have serious heart disease ( patients who have apparent heartfailure or myocardial infarction within 3 months) 5) patients who have serious pancreatic disease 6) patients with cancer 7) anemic patients (Hb is less than 11g/dL) 8) patients with thrombocytepenia (Platelet count is less than 100000/mm3) 9) patients with serious diabetic complications including progressed neutopathy and proliferative retinopathy 10) patietns with serious infection, inflammation, or injuary. pre- or post- operative state 11) patients who have inflammatory bowel disease, ulcer in bowel, ileus and high risk for ileus 12) patinets with chronic bowel diseases which have probability to induce malabsorption syndrome 13) patients who has the disease which is deteriorated with increase of gas in bowel 14) heavy alcohol drinker (patients who drink more than 480mL of Japanese Sake, 2L of beer, 180mL of whisky, 360mL of wine, or 360mL of Shochu per day) 15) patients who are pregnant, hope to be pregnant, or are in lactation period 16) patients who have viral infection (HBV,HCV) 17) patients who are not applicable to this study judged by the medical doctor.

Design outcomes

Primary

MeasureTime frame
1. efficacy of addition of glimepiride on glyceic control 2. influence of addition of glimepiride on pancreatic beta cell function 3. preventive effect of addition of glimepiride on atherosclerosis (Using IMT as surrogate endopoint)

Countries

Japan

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026