MD-Logic Artificial Pancreas for Automatic Type 1 Diabetes Meals Management

NCT01901913 | Completed

• 1 other identifier: rmc007418ctil
• Study Type: interventional
• Target: 26
• Locations: 1 country
• Sites: 1

Brief Summary

The MDLAP (MD-Logic Artificial Pancreas)system is as an automatic system to regulate glucose levels by delivery of insulin operable in clinical trial settings. The safety of the system was proved in previous inpatient and outpatient trials in large number of patients. In the current study we aim to optimize post-prandial closed-loop glycemic control by developing an automated MD-bolus calculator and to evaluate its safety and efficacy in controlling postprandial blood glucose when used together with the MD-Logic artificial pancreas system in type 1 diabetes patients. The study will consist of a pilot study with two segments and a main study segment. The aim of each segment is detailed below:

1. 1.Pilot Study - Segment 1 - Hybrid meal bolus ratio The aim of this segment is to evaluate the efficacy and safety of different pre-meal bolus dosing compared to full closed-loop operation with no meal announcement.
2. 2.Pilot Study - Segment 2 - Insulin dosing during meal In this segment we would like to test the optimal distribution of insulin delivery during the meal.
3. 3.Main study - Segment 3 - Automatic bolus calculator In this main segment of the study we will use the results and conclusions from the previous two pilot segments to develop the MD-Bolus Calculator for closed-loop control use. The safety and efficacy of this automated insulin bolus calculator will be tested in a randomized cross-over study that will compare postprandial glycemic control under MDLAP with and without the use of the MD-Bolus Calculator.

Conditions

Type 1 Diabetes

Keywords

Type 1 Diabetes; Artificial pancreas; Closed loop

Outcome Measures

Primary Outcomes (1)

• Area under the curve above 180 mg/dl (10 mmol/l)

  4 hours postprandial

Secondary Outcomes (6)

• Time within range of 70-180 mg/dl over 4 hours from the beginning of the meal

  4 hours postprandial

• The incremental glucose rise from premeal to peak postprandial level

  4 hours postprandial

• Number of hypoglycemic events below 70 mg/dl (3.9 mmol/l)

  4 hours postprandial

• The percentage of subjects who reached the desired glucose target (70-180 mg/dl) 4 hours postprandial.

  4 hours postprandial

• Percentage of time spent below 70 mg/dl (3.9mmol/l)

  4 hours postprandial

Study Arms (2)

MD-bolus calculator for pre meal bolus

EXPERIMENTAL

closed loop session with MD-bolus calculator for pre-meal bolus.

Device: MD-bolus calculator for pre-meal bolus

No MD-bolus calculator for pre-meal bolus

ACTIVE COMPARATOR

closed loop session without MD-bolus calculator for pre-meal bolus

Device: No MD-bolus calculator for pre-meal bolus

Interventions

MD-bolus calculator for pre-meal bolus DEVICE

MD-bolus calculator for pre meal bolus

No MD-bolus calculator for pre-meal bolus DEVICE

No MD-bolus calculator for pre-meal bolus

Eligibility Criteria

• Age: 14 Years - 25 Years
• Sex: all
• Healthy Volunteers: No
• Age Groups: Child (0-17), Adult (18-64)

You may qualify if:

• Diabetes type 1
• Age 14-25 years
• \>1yr since diagnosis
• Insulin infusion pump therapy for at least 3 months
• BMI \< 95th percentile for age and sex
• Patients willing to follow study instructions

You may not qualify if:

• Any condition that influence intestinal absorption or motility such as diabetic gastroparesis, celiac disease or malabsorptive states that could affect postprandial glucose absorption.
• any episode of diabetic ketoacidosis within the month prior to study entry and/or severe hypoglycaemia resulting in seizure or loss of consciousness in the month prior to enrolment
• any concomitant disease that may influence metabolic control
• participation in any other interventional study
• known or suspected allergy to trial products
• any significant diseases (such as preexisting seizures or epilepsy) or conditions including psychiatric disorders, eating disorder and substance abuse that in the opinion of the investigator is likely to affect the subjects ability to complete the study or compromise patients safety
• Female subject who is pregnant or planning to become pregnant within the planned study duration.

Sponsors & Collaborators

• Rabin Medical Center: lead

Study Sites (1)

Schneider Children's Medical Center

Petah Tikva, Petah-Tikva, 49202, Israel

Location

MeSH Terms

Conditions

Diabetes Mellitus, Type 1

Condition Hierarchy (Ancestors)

Diabetes Mellitus; Glucose Metabolism Disorders; Metabolic Diseases; Nutritional and Metabolic Diseases; Endocrine System Diseases; Autoimmune Diseases; Immune System Diseases

Study Design

• Study Type: interventional
• Phase: not applicable
• Allocation: RANDOMIZED
• Masking: NONE
• Purpose: TREATMENT
• Intervention Model: CROSSOVER
• Sponsor Type: OTHER
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: July 9, 2013
• First Posted: July 17, 2013
• Study Start: October 1, 2013
• Primary Completion: April 1, 2015
• Study Completion: April 1, 2015
• Last Updated: April 16, 2015

Record last verified: 2014-11

Locations

IL (1)