Diabetes mellitus
Conditions
Interventions
Using the combination therapy with telemonitoring and individual insulin titration system (NOCTIS) during four months
Sponsors
The Jikei University School of Medicine
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: (a) Diabetes (over 20 and under 75 years of age) (b) patients who regularly use self-care insulin (c) HbA1c (NGSP) over 7.0% and under 10.0% (d) using self monitoring of blood glucose (e) patients who are able to visit our hospital every month (f) having e-mail address and mobile phone (g) patients who have received adequate explanation of the contents of the trial and given their written consent.
Exclusion criteria
Exclusion criteria: a) having severe renal dysfunction (serum Cr > 2.5 mg/dl) b) having severe liver dysfunction (3 X the upper limit of normal) c) having severe infection, severe trauma, or pre and post operation d) having diabetic ketosis, diabetic coma, or insulin-dependent diabetes mellitus e) heavy drinker f) being pregnant g) having malignancy h) having visual disorder i) being unsuitable for participation in the trial for any reason, according to the investigators
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| HbA1c | — |
Countries
Japan
Contacts
Public ContactIuchi Hiroyuki
The Jikei University Katsushika Medical Center Division of Diabetes, Metabolism and Endocrinology, Department of Internal Medicine
Outcome results
None listed