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Clinical Trials/NCT02928016
NCT02928016
Completed
Not Applicable

Effectiveness of the Carbohydrate Counting Method on Postprandial Glucose Concentrations After Consumption of Mixed Meals in Adults With Type 1 Diabetes

Agricultural University of Athens0 sites120 target enrollmentSeptember 2014
ConditionsType 1 Diabetes

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Type 1 Diabetes
Sponsor
Agricultural University of Athens
Enrollment
120
Primary Endpoint
Capillary blood glucose
Status
Completed
Last Updated
9 years ago

Overview

Brief Summary

In a randomized, cross-over designed study, the investigators examined the effectiveness of the carbohydrate counting method after consumption of mixed meals typical of the Greek cuisine with various protein and fat contents in a sample of people with type 1 diabetes (DM1). The investigators also tried to further explore the effects of additional extra virgin olive oil (11 ml) on the glycemic response.

Detailed Description

A total of 20 adults with type 1 diabetes on intensive insulin therapy consumed three mixed meals at noon between 1200 and 1300 hours, with and without the addition of 11 ml extra virgin oil, in random order. One week before entering the study, participants kept a detailed 7-day weighed food record with fingerprick blood glucose measurements pre-and-2hour post-meals for calculation of their carbohydrate (g) to insulin (units) ratio. Moreover, the individual correction factor was calculated. Thereafter, insulin requirements for the test meals were calculated based on the carbohydrate content of each dish and according to the personalised carbohydrate to insulin ratio. Postprandial glycemia was measured in capillary blood glucose samples at 30min intervals over 195min. For 24hr before each testing session, participants were asked to refrain from the consumption of alcohol and to maintain their usual physical activity pattern. On the day of testing, subjects were asked to consume their usual breakfast and abstain from food for at least 2 hours before their appointment. If blood glucose was \>7.2 mmol/l at 1200, insulin was administered based on the individualised correction factor. If blood glucose was \>10 mmol/l at the beginning of the testing session, insulin was administered to correct it and the subject was asked to return on another day. if hypoglycaemia occurred (defined as blood glucose level \<3.8 mmol/l), the test session was stopped, the event was recorded and the patient treated appropriately. The on target 2hour postprandial blood glucose level was set between 3.9 and 10 mmol/l. Anthropometric measurements (body weight, waist and hip circumferences) were performed at every visit.

Registry
clinicaltrials.gov
Start Date
September 2014
End Date
June 2016
Last Updated
9 years ago
Study Type
Interventional
Study Design
Crossover
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Aimilia Papakonstantinou

Lecturer in Nutrition and Metabolism Unit of Human Nutrition Dept of Food Science and Human Nutrition Agricultural University Of Athens

Agricultural University of Athens

Eligibility Criteria

Inclusion Criteria

  • Patients with type 1 diabetes
  • Intensive insulin therapy
  • HbA1c \< 10%
  • \>2 years with diabetes

Exclusion Criteria

  • Food allergies
  • Diabetic neuropathy
  • Kidney disease
  • Hematological disturbances
  • Liver disease
  • Uncontrolled hypo- or hyperthyroidism
  • Arrhythmia
  • Heart disease
  • Serious mental illness

Outcomes

Primary Outcomes

Capillary blood glucose

Time Frame: 195 minutes

Clinically useful change in capillary blood glucose, defined as the restoration of glucose within normal limits during the first two hours and until the end of the trial

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