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N/A N=235 Randomized Treatment

Point-of-Care Glucose Testing and Insulin Supplementation

Diabetes

Enrolled (actual)
235
Serious AEs
0.0%
Results posted
Aug 2014
Primary outcome: Primary: Mean Fasting Blood Glucose — 162; 157 mg/dL

Study Design & Population

Study type
Interventional
Phase
N/A
Interventions
Bedtime insulin Aspart (Novolog) (Drug)
Age
Adult, Older Adult · 18+ yrs
Sex
All
Sponsor
Emory University
Primary completion
Dec 2013

Outcome Measures

OutcomeResultp-value
PRIMARY
Mean Fasting Blood Glucose
162; 157
SECONDARY
Mean Daily BG
8.8; 8.7
SECONDARY
Number of Hypoglycemia (BG < 70 mg/dl)
32; 26
SECONDARY
Daily Dose of Insulin
39; 44
SECONDARY
Length of Hospital Stay
7; 6
SECONDARY
Hospital Mortality
0; 1
SECONDARY
Nosocomial Infections (CDC)
0; 0
SECONDARY
Pneumonia
1; 0
SECONDARY
Bacteremia
0; 0
SECONDARY
Participants Will be Followed for the Duration of Hospital Stay, an Expected Average of 6 Days
1; 0
SECONDARY
Acute Renal Failure [Rise >50% of Baseline or Creatinine >2.5 mg/dl]
4; 4
SECONDARY
Number of BG Within Target
76; 74
SECONDARY
Number of Subjects With BG > 300 mg/dL
19; 13

Summary

Capillary point-of-care (POC) testing is advocated as a valuable aid in the management of diabetes and hyperglycemia in the hospital setting. POC testing aims at collecting information on BG levels at different time points during the day in order to assess glycemic control and to guide insulin adjustment/correction doses. Although POC testing provides insights into day-to-day excursions in BG levels, bedtime BG testing triggers the use of insulin supplements that may result in increased frequency of hypoglycemia and is expensive with an estimated annual cost in hospitals of several hundreds of millions of dollars in the U.S. Accordingly, this pilot study aims to assess the utility of POC and insulin supplementation (correction doses) at bedtime in improving glycemic control and in preventing hypoglycemia in non-ICU patients with type 2 diabetes mellitus (T2DM). A total of 250 non-ICU medical and surgical patients treated with basal bolus regimen will undergo POC testing before meals and bedtime (standard of care) and half of the patients will receive insulin correction doses at bedtime for BG > 140 mg/dL following a sliding scale protocol, while the other half will be followed without insulin supplementation at bedtime except for extreme hyperglycemia (BG > 350 mg/dl). Patients will be recruited at Emory University Hospital and Grady Memorial Hospital.

Eligibility Criteria

Inclusion Criteria

  • Male and female patients with a known history of T2DM for > 3 months
  • Age 18-80 years
  • Home treatment with either diet alone, any combination of oral antidiabetic agents, non-insulin injectables or insulin therapy
  • BG > 140 mg and < 400 mg/dL without laboratory evidence of diabetic ketoacidosis

Exclusion Criteria

  • Hyperglycemia without a history of diabetes
  • Acute critical illness admitted to the ICU or expected to require ICU admission
  • Receiving continuous insulin infusion
  • Clinically relevant hepatic disease
  • Patients on corticosteroid therapy
  • Patients with creatinine ≥ 3.5 mg/dl
  • Subjects unable to sign consent
  • Pregnancy
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT01702311). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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