None listed
Conditions
Brief summary
The aim is to determine whether 4 fingerprick BGLs routinely performed at nominal times of 0700, 1200, 1700 (these three timeslots are just before meals) and 2100 hours accurately assess the efficacy and safety of basal bolus insulin in hospitalized patients.
Interventions
Determine whether 4 fingerprick capillary blood glucose levels taken at routine sampling times of 0700, 1200, 1700 and 2100 hours over a 24 hour period during a hospital admission, as measured by standard hospital ward glucometers, accurately reflects glucose concentrations determined by continuous glucose monitoring. The duration of sampling will be up to 2 full consecutive days with a minimum of one full day (midnight to midnight). This will be in a population of known diabetic patients receiving the standard basal bolus insulin regimen, which is used for patients requiring temporary intensified blood glucose management during admission. Patient recruitment is planned until August 2012.
Sponsors
Eligibility
Inclusion criteria
Any hospitalised diabetic inpatient requiring basal-bolus managent for glycaemic control
Exclusion criteria
Unable to provide wrtiien informed consent. Precluded from CGMS use eg requires MRI or abdo surgery during study period