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Clinical Trials/JPRN-UMIN000014417
JPRN-UMIN000014417
Completed
未知

Effects of Linagliptin on Hypoglycemia :Hypoglycemic Clamp Test in Japanese T2DM Patients - Hypoglycemic Clamp Test in Japanese T2DM Patients

Kansai Electric Power Hospital0 sites35 target enrollmentJuly 1, 2014
ConditionsType 2 diabetes

Overview

Phase
未知
Intervention
Not specified
Conditions
Type 2 diabetes
Sponsor
Kansai Electric Power Hospital
Enrollment
35
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
July 1, 2014
End Date
April 20, 2015
Last Updated
2 years ago
Study Type
Interventional
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • (1\)Patients with diabetes requiring insulin therapy (insulin intensive therapy, T1DM, etc) (2\)Patients currently treated with Insulin, DPP\-4inhibitor, GLP\-1 receptor agonist within 4 weeks and/or treated with Pioglitazon within 12weeks (3\)Patients currently treated with alpha blocker, beta blocker, selective serotonin reuptake inhibitors (4\)Patients with history of cerebrovascular and cardiovascular disease (5\)Patients with heart failure with NYHA I\-IV (6\)Patients with renal dysfunction (7\)Patients with severe hepatic dysfunction (8\)Patients with history of pancreatitis (9\)Patients with diabetic retinopathy (proliferative retinopathy, vitreous hemorrhage and more severe condition) (10\)Patients with autonomic neuropathy (11\)Patients with a history of surgery of gastrointestinal tract (12\)Patients with malignant tumor (13\)Patients with severe infection, in the perioperative period or with serious injury (14\)Excessive alcohol intake (15\)Patients with hemoglobin (Hb) \<13\.0g/dL(male), \<12\.5g/dL(female) (16\)Patients found ineligible as a study patient according to the discretion of the investigator or sub\-investigator (17\)Patients participating in other clinical studies (18\)Pregnant or possibly pregnant women (19\)Patients judged as inadequate to participate in present study by investigator or sub\-investigator

Outcomes

Primary Outcomes

Not specified

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