Type 2 Diabetes Mellitus Clinical Trial
Official title:
Insulin Scheme for Glycemic Control in Non-critical Hospitalized Patients With Type 2 Diabetes in the Context of a Health System in Mexico.
Verified date | November 2021 |
Source | Universidad de Guanajuato |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The aim of the study is to determine differences in glycemic control between a basal-bolus scheme insulin and NPH scheme insulin in a population of hospitalized patients with type 2 diabetes in a Noncritical Care Facility in Mexico. Patients with a recent diagnosis of type 2 and patients on treatment with oral hypoglycaemic agents and insulin or only insulin were included. The primary outcome of the study is to determine difference in efficacy and security between a basal-bolus scheme insulin and NPH scheme insulin in patients with type 2 diabetes hospitalized in non-critical areas in a hospital in Mexico
Status | Completed |
Enrollment | 75 |
Est. completion date | July 1, 2018 |
Est. primary completion date | July 1, 2018 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 100 Years |
Eligibility | Inclusion Criteria: - Patients between 18 and 100 years old. - History of type 2 diabetes mellitus (DM2) or that upon admission is diagnosed by values of glycated haemoglobin (HbA1) > 6.5% - Fasting central glucose before randomization between 140mg/dl and 400mg/dl - Non-critical patients hospitalized in the service of Internal Medicine (MI), General Surgery (CG) and Traumatology (TyO). - Patients receiving a diabetic diet orally - Treated with diet alone, o any combination of oral anti-diabetic agents or insulin treatment with any dosage before admission. Exclusion Criteria: - Parenteral nutrition - Hyperglycemia without a known history of diabetes - Impaired renal function (glomerular filtration rate less than 30) - Diabetic ketoacidosis and hyperosmolar state - Type 1 Diabetes mellitus - Pregnancy - Patients on treatment with more than 10mg prednisone or steroid boluses. - Known hypopituitarism or adrenal insufficiency - Hyperglycaemia due to stress (negative antecedent of DM2, hyperglycemia and HbA1 <6.5) - Severe liver disease (Child-Pugh C score) - Acute pancreatitis - Patients with sepsis or multiple organ failure - Candidates for intensive care unit |
Country | Name | City | State |
---|---|---|---|
Mexico | Hospital General de León | León | Guanajuato |
Lead Sponsor | Collaborator |
---|---|
Universidad de Guanajuato |
Mexico,
Christensen MB, Gotfredsen A, Nørgaard K. Efficacy of basal-bolus insulin regimens in the inpatient management of non-critically ill patients with type 2 diabetes: A systematic review and meta-analysis. Diabetes Metab Res Rev. 2017 Jul;33(5). doi: 10.1002/dmrr.2885. Epub 2017 Feb 23. Review. — View Citation
Umpierrez GE, Smiley D, Hermayer K, Khan A, Olson DE, Newton C, Jacobs S, Rizzo M, Peng L, Reyes D, Pinzon I, Fereira ME, Hunt V, Gore A, Toyoshima MT, Fonseca VA. Randomized study comparing a Basal-bolus with a basal plus correction insulin regimen for the hospital management of medical and surgical patients with type 2 diabetes: basal plus trial. Diabetes Care. 2013 Aug;36(8):2169-74. doi: 10.2337/dc12-1988. Epub 2013 Feb 22. — View Citation
Umpierrez GE, Smiley D, Jacobs S, Peng L, Temponi A, Mulligan P, Umpierrez D, Newton C, Olson D, Rizzo M. Randomized study of basal-bolus insulin therapy in the inpatient management of patients with type 2 diabetes undergoing general surgery (RABBIT 2 surgery). Diabetes Care. 2011 Feb;34(2):256-61. doi: 10.2337/dc10-1407. Epub 2011 Jan 12. — View Citation
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Differences in the Mean Daily Blood Glucose Between a Basal-bolus Scheme and NPH Schemes of Insulin. | To determine the differences in the mean daily blood glucose measured in mg/dl, between a basal-bolus scheme and NPH schemes of insulin measured by the mean daily blood glucose. | Fasting blood glucose was taken every day, before breakfast, up to 4 weeks; postprandial glucose was taken every day, 2 hours after breakfast, 2 hours after lunch, and 2 hours after dinner, up to 4 weeks; glucose early morning was taken 3 am, up to 4 week | |
Secondary | the Number of Participants With Mild and Severe Hypoglycemic Events | To measure the number of participants with mild and severe hypoglycemic events | Duration of hospital stay, up to 4 weeks. | |
Secondary | Number of Participants With Sustained Glycemic Control During Hospital Stay | Sustained glycemic control were the number of participants who not had: discharged before sustained control, critical status suspension, death before control, bad attachment to the protocol, interruption due to more than 2 hypoglycemic events during their hospital stay. | blood glucose was taken every day, up to 4 weeks. |
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