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Insulin Pump Therapy in Adolescents With Newly Diagnosed Type 1 Diabetes (T1D)

Primary Purpose

Diabetes Mellitus, Insulin-Dependent

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Insulin pump therapy
Multiple daily injections using insulin glargine + rapid acting analog
Sponsored by
Nemours Children's Clinic
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Diabetes Mellitus, Insulin-Dependent focused on measuring type 1 diabetes, diabetes, new onset, CSII, insulin sensitivity, beta cell function, beta cell preservation

Eligibility Criteria

12 Years - 17 Years (Child)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Male or female patient between the age of 12 and 17 years inclusive at time of entry into study (i.e., after their 12th but before their 18th birthday) Type 1 diabetes mellitus for no more than 10 days pubertal (Tanner stage 2 or above) The patient and parents or guardians should be able to do simple math calculations (necessary for pump management) Parent or legal guardian must give signed informed consent Exclusion Criteria: No other chronic medical conditions (well-controlled thyroid disease is OK, and mild asthma is OK if the patient is not on chronic inhaled or oral daily corticosteroids) Exceptional psychological stress, more than expected for circumstances of having the new diagnosis of diabetes Inability or unwillingness to comply with requirements of the protocol

Sites / Locations

  • Nemours Children's Clinic

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Pump therapy (CSII)

Multiple daily injections (MDI)

Arm Description

Use of pump therapy

Use of MDI (basal bolus therapy with glargine)

Outcomes

Primary Outcome Measures

Insulin Sensitivity
Insulin sensitivity - glucose infusion rate (GIR) obtained from hyperinsulinemic-euglycemic clamp. Higher GIR reflects higher insulin sensitivity, lower GIR reflects lower insulin sensitivity.
Beta Cell Function
Beta cell function as assessed by peak c-peptide using mixed meal tolerance testing

Secondary Outcome Measures

Hemoglobin A1c
Hemoglobin A1c (HbA1c) (%)
Percent Body Fat
Percent body fat based on DEXA scan (%BF)

Full Information

First Posted
July 26, 2006
Last Updated
July 6, 2023
Sponsor
Nemours Children's Clinic
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1. Study Identification

Unique Protocol Identification Number
NCT00357890
Brief Title
Insulin Pump Therapy in Adolescents With Newly Diagnosed Type 1 Diabetes (T1D)
Official Title
A Pilot Study of the Effect of Continuous Subcutaneous Insulin Infusion in Adolescents With Newly-diagnosed Type 1 Diabetes on Insulin Resistance, Beta-cell Function and the Honeymoon Period.
Study Type
Interventional

2. Study Status

Record Verification Date
July 2023
Overall Recruitment Status
Completed
Study Start Date
December 2005 (undefined)
Primary Completion Date
October 2014 (Actual)
Study Completion Date
October 2014 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Nemours Children's Clinic

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Within 4 weeks after diagnosis of type 1 diabetes, 10 subjects (pubertal males, 12-17 years old) will be randomized to either receive multiple daily injection (MDI) using Lantus insulin, or continuous subcutaneous insulin infusion (CSII; pump therapy). The study evaluates how these modes of therapy affect insulin sensitivity (measured by the euglycemic-hyperinsulinemic clamp studies and adiponectin concentration changes) and beta cell function (measured by mixed meal tolerance testing).
Detailed Description
Within 4 weeks after diagnosis of type 1 diabetes, 10 subjects (pubertal males, 12-17 years old) will be randomized to either receive multiple daily injection (MDI) using Lantus insulin, or continuous subcutaneous insulin infusion (CSII; pump therapy). The proposed protocol compares the changes in diabetes control between pump therapy and MDI treatment groups. More importantly, however, the study evaluates how these modes of therapy may affect the honeymoon period and glycemic control, specifically focusing on changes in insulin sensitivity (measured by the euglycemic-hyperinsulinemic clamp studies and adiponectin concentration changes) and beta cell function (measured by mixed meal tolerance testing). Demonstrating that pump therapy at the time of diagnosis of type 1 diabetes prolongs the honeymoon phase by improving insulin sensitivity and beta cell function may have important therapeutic implications that could influence the standard of care in pediatric diabetes.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Diabetes Mellitus, Insulin-Dependent
Keywords
type 1 diabetes, diabetes, new onset, CSII, insulin sensitivity, beta cell function, beta cell preservation

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
12 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Pump therapy (CSII)
Arm Type
Experimental
Arm Description
Use of pump therapy
Arm Title
Multiple daily injections (MDI)
Arm Type
Active Comparator
Arm Description
Use of MDI (basal bolus therapy with glargine)
Intervention Type
Device
Intervention Name(s)
Insulin pump therapy
Other Intervention Name(s)
Continuous subcutaneous insulin infusion (CSII)
Intervention Description
CSII initiated within 1 month of diagnosis
Intervention Type
Drug
Intervention Name(s)
Multiple daily injections using insulin glargine + rapid acting analog
Other Intervention Name(s)
MDI using glargine plus a rapid acting analog
Intervention Description
MDI as control
Primary Outcome Measure Information:
Title
Insulin Sensitivity
Description
Insulin sensitivity - glucose infusion rate (GIR) obtained from hyperinsulinemic-euglycemic clamp. Higher GIR reflects higher insulin sensitivity, lower GIR reflects lower insulin sensitivity.
Time Frame
24 months
Title
Beta Cell Function
Description
Beta cell function as assessed by peak c-peptide using mixed meal tolerance testing
Time Frame
24 months
Secondary Outcome Measure Information:
Title
Hemoglobin A1c
Description
Hemoglobin A1c (HbA1c) (%)
Time Frame
24 months
Title
Percent Body Fat
Description
Percent body fat based on DEXA scan (%BF)
Time Frame
24 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
12 Years
Maximum Age & Unit of Time
17 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Male or female patient between the age of 12 and 17 years inclusive at time of entry into study (i.e., after their 12th but before their 18th birthday) Type 1 diabetes mellitus for no more than 10 days pubertal (Tanner stage 2 or above) The patient and parents or guardians should be able to do simple math calculations (necessary for pump management) Parent or legal guardian must give signed informed consent Exclusion Criteria: No other chronic medical conditions (well-controlled thyroid disease is OK, and mild asthma is OK if the patient is not on chronic inhaled or oral daily corticosteroids) Exceptional psychological stress, more than expected for circumstances of having the new diagnosis of diabetes Inability or unwillingness to comply with requirements of the protocol
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Larry A Fox, MD
Organizational Affiliation
Nemours Chidlren's Clinic
Official's Role
Principal Investigator
Facility Information:
Facility Name
Nemours Children's Clinic
City
Jacksonville
State/Province
Florida
ZIP/Postal Code
32207
Country
United States

12. IPD Sharing Statement

Learn more about this trial

Insulin Pump Therapy in Adolescents With Newly Diagnosed Type 1 Diabetes (T1D)

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