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Insulin Pump vs Multiple Daily Injections of Insulin and Glyco-metabolic Control in Type 1 Diabetic Patients (METRO)

Primary Purpose

Type 1 Diabetes Mellitus

Status
Recruiting
Phase
Phase 4
Locations
Italy
Study Type
Interventional
Intervention
Insulin pump
Insulin injections
Sponsored by
University of Campania "Luigi Vanvitelli"
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Type 1 Diabetes Mellitus focused on measuring type 1 diabetes, transition, CSII, MDI, glycemic control, glucose variability

Eligibility Criteria

18 Years - 30 Years (Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • T1DM for at least 12 months
  • persistent HbA1c levels ≥ 7.5% (58 mmol/mol) despite optimized education therapy,
  • recurrent severe hypoglycemic episodes or high glucose variability
  • willingness to wear the insulin pump

Exclusion Criteria:

  • previous use of insulin pump
  • pregnancy or planning to become pregnant in the next 2 years,
  • lack of ability to use the study devices
  • history of severe chronic diseases
  • recent or concomitant use of corticosteroids
  • drug or alcohol abuse
  • psychiatric complaints that interfere with the correct use of the devices

Sites / Locations

  • Unit of DiabetesRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Active Comparator

Arm Label

Insulin pump

Insulin injections

Arm Description

Insulin Pump with rapid acting insulin analog lispro

Four injections of insulin daily consisting in three bolus of a rapid-acting analog lispro or aspart before breakfast, lunch and dinner and one injection at bed-time of basal insulin glargine or degludec

Outcomes

Primary Outcome Measures

HbA1c change
Within and between groups difference in HbA1c levels
Change in mean amplitude glucose excursions (MAGE
Within and between groups difference in glucose variability measured as mean amplitude of glucose excursions (MAGE).
Change in coefficient of variation (CV)
Within and between groups difference in glucose variability measured as coefficient of variation (CV).
Change in standard deviation (SD) of mean glucose levels
Within and between groups difference in glucose variability measured as standard deviation (SD) of mean glucose levels
Change in glucose variability
Within and between groups difference in time in the euglycemic range, defined as the minutes per day spent in glucose levels ranging between 70-180 mg/dL

Secondary Outcome Measures

Occurrence of hypoglycemic events
Number of events of mild hypoglycemia (glucose levels below 70 mg/dl), or severe hypoglycemia (below 54 mg/dl or each episode of low glucose levels requiring assistance)
Change in weight
Change in lipid profile
Difference between groups in total cholesterol, LDL-cholesterol, HDL-cholesterol, triglycerides
Total daily insulin doses/Kg
Diabetes treatment satisfaction
In order to measure satisfaction with diabetes treatment regimens, we used the self-reported Diabetes Treatment Satisfaction Questionnaire. This instrument aims to assess levels of satisfaction in subjects using different treatment strategies. The questionnaire consists of eight questions: six questions addresses general satisfaction with a score from 0 to 6 for each question (0 = worst), that has to be computed in a total score ranging from 0 (=worst) to 36 (=best); among the remaining two questions, which has to be computed separately as two subscales, one concerns the perception of hyperglycemic events and another the perception of hypoglycemic events, both with a score from 0 (none of the time) to 6 (most of the time).

Full Information

First Posted
February 19, 2018
Last Updated
March 13, 2018
Sponsor
University of Campania "Luigi Vanvitelli"
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1. Study Identification

Unique Protocol Identification Number
NCT03463564
Brief Title
Insulin Pump vs Multiple Daily Injections of Insulin and Glyco-metabolic Control in Type 1 Diabetic Patients
Acronym
METRO
Official Title
Effects of Insulin Pump Versus Multiple Daily Injections of Insulin on Glycemic and Metabolic Control in Type 1 Diabetic Patients Transitioned to the Adult Center: the Management and Technology for Transition Study (METRO)
Study Type
Interventional

2. Study Status

Record Verification Date
March 2018
Overall Recruitment Status
Recruiting
Study Start Date
January 2016 (undefined)
Primary Completion Date
December 2026 (Anticipated)
Study Completion Date
December 2026 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Campania "Luigi Vanvitelli"

4. Oversight

5. Study Description

Brief Summary
The transition from the Pediatric clinic to the adult care is a challenging period for young adults with type 1 diabetes, due to the high risk of poor glycemic control. Achieving the glycemic target without hypoglycemia and/or large glucose excursions is of paramount importance for type 1 diabetic patients, who have high variability of daily glucose levels . Both insulin pump therapy and multiple daily injections of insulin are recommended strategy to achieve glycemic control in type 1 diabetes; however, no studies investigated the effects of insulin pump vs insulin injections on glycol-metabolic outcomes in the transition phase. The aim of this study was to evaluate the effects of continuous subcutaneous insulin infusion (CSII) therapy, as compared with multiple daily injections of insulin (MDI), on glycemic and metabolic control, in young type 1 diabetic patients transitioned to the adult diabetes care.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Type 1 Diabetes Mellitus
Keywords
type 1 diabetes, transition, CSII, MDI, glycemic control, glucose variability

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
150 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Insulin pump
Arm Type
Active Comparator
Arm Description
Insulin Pump with rapid acting insulin analog lispro
Arm Title
Insulin injections
Arm Type
Active Comparator
Arm Description
Four injections of insulin daily consisting in three bolus of a rapid-acting analog lispro or aspart before breakfast, lunch and dinner and one injection at bed-time of basal insulin glargine or degludec
Intervention Type
Device
Intervention Name(s)
Insulin pump
Other Intervention Name(s)
CSII
Intervention Description
Continuous subcutaneous insulin infusion consisting of the delivery of insulin lispro as basal rate and boluses administered before meals.
Intervention Type
Drug
Intervention Name(s)
Insulin injections
Other Intervention Name(s)
MDI
Intervention Description
Four injections of insulin daily consisting in three bolus of a rapid-acting analog lispro or aspart before breakfast, lunch and dinner and one injection of insulin glargine or degludec at bed-time of basal insulin
Primary Outcome Measure Information:
Title
HbA1c change
Description
Within and between groups difference in HbA1c levels
Time Frame
Baseline, 6 months, 12 months, 24 months
Title
Change in mean amplitude glucose excursions (MAGE
Description
Within and between groups difference in glucose variability measured as mean amplitude of glucose excursions (MAGE).
Time Frame
Baseline, 6 months, 12 months, 24 months
Title
Change in coefficient of variation (CV)
Description
Within and between groups difference in glucose variability measured as coefficient of variation (CV).
Time Frame
Baseline, 6 months, 12 months, 24 months
Title
Change in standard deviation (SD) of mean glucose levels
Description
Within and between groups difference in glucose variability measured as standard deviation (SD) of mean glucose levels
Time Frame
Baseline, 6 months, 12 months, 24 months
Title
Change in glucose variability
Description
Within and between groups difference in time in the euglycemic range, defined as the minutes per day spent in glucose levels ranging between 70-180 mg/dL
Time Frame
Baseline, 6 months, 12 months, 24 months
Secondary Outcome Measure Information:
Title
Occurrence of hypoglycemic events
Description
Number of events of mild hypoglycemia (glucose levels below 70 mg/dl), or severe hypoglycemia (below 54 mg/dl or each episode of low glucose levels requiring assistance)
Time Frame
Through study completion, an average of 1 year
Title
Change in weight
Time Frame
Baseline, 12 months, 24 months
Title
Change in lipid profile
Description
Difference between groups in total cholesterol, LDL-cholesterol, HDL-cholesterol, triglycerides
Time Frame
Baseline, 12 months, 24 months
Title
Total daily insulin doses/Kg
Time Frame
Baseline, 12 months, 24 months
Title
Diabetes treatment satisfaction
Description
In order to measure satisfaction with diabetes treatment regimens, we used the self-reported Diabetes Treatment Satisfaction Questionnaire. This instrument aims to assess levels of satisfaction in subjects using different treatment strategies. The questionnaire consists of eight questions: six questions addresses general satisfaction with a score from 0 to 6 for each question (0 = worst), that has to be computed in a total score ranging from 0 (=worst) to 36 (=best); among the remaining two questions, which has to be computed separately as two subscales, one concerns the perception of hyperglycemic events and another the perception of hypoglycemic events, both with a score from 0 (none of the time) to 6 (most of the time).
Time Frame
Baseline, 12 months, 24 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
30 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: T1DM for at least 12 months persistent HbA1c levels ≥ 7.5% (58 mmol/mol) despite optimized education therapy, recurrent severe hypoglycemic episodes or high glucose variability willingness to wear the insulin pump Exclusion Criteria: previous use of insulin pump pregnancy or planning to become pregnant in the next 2 years, lack of ability to use the study devices history of severe chronic diseases recent or concomitant use of corticosteroids drug or alcohol abuse psychiatric complaints that interfere with the correct use of the devices
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Katherine Esposito
Phone
+390815665031
Email
katherine.esposito@unicampania.it
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Katherine Esposito
Organizational Affiliation
University of Campania "Luigi Vanvitelli"
Official's Role
Principal Investigator
Facility Information:
Facility Name
Unit of Diabetes
City
Naples
ZIP/Postal Code
80138
Country
Italy
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Katherine Esposito
Phone
+390815665031
Email
katherine.esposito@unicampania.it
First Name & Middle Initial & Last Name & Degree
Katherine Esposito
First Name & Middle Initial & Last Name & Degree
Giuseppe Bellastella
First Name & Middle Initial & Last Name & Degree
Maria Ida Maiorino
First Name & Middle Initial & Last Name & Degree
Michela Petrizzo

12. IPD Sharing Statement

Plan to Share IPD
No

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Insulin Pump vs Multiple Daily Injections of Insulin and Glyco-metabolic Control in Type 1 Diabetic Patients

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