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A Study of Two Versus Three Daily Injections in Children and Adolescents With Newly Diagnosed Type 1 Diabetes

Primary Purpose

Diabetes Mellitus, Type 1

Status
Completed
Phase
Phase 2
Locations
Canada
Study Type
Interventional
Intervention
Twice Daily versus Three Times Daily Insulin Injections
Sponsored by
Children's Hospital of Eastern Ontario
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional treatment trial for Diabetes Mellitus, Type 1 focused on measuring Diabetes Mellitus, Type 1, Child, Adolescent, Disease Management, Newly Diagnosed, Hemoglobin A, Glycosylated

Eligibility Criteria

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

Inclusion Criteria: New onset type 1 diabetes Less than 48 hours since first insulin injection Child and/or parent able to read and write English Family intends to continue treatment at our institution for the next two years Informed consent from adolescents greater than 16 years of age, or if less than 16 years, informed consent from the parent/guardian with assent from the child. Exclusion Criteria: Chronic medical conditions other than treated hypothyroidism or mild asthma Concerns of the diabetes team regarding future treatment adherence making twice daily insulin preferable to the split evening injection regimen (e.g., cognitive impairment, severe family dysfunction).

Sites / Locations

  • Children's Hospital of Eastern Ontario

Outcomes

Primary Outcome Measures

* Hemoglobin A1c over the first 24 months of diabetes

Secondary Outcome Measures

* Frequency of hypoglycemia (mild and severe) over the first 24 months of diabetes
* Frequency of morning hyperglycemia over the first 24 months of diabetes
* Residual c-peptide at two years post diagnosis (stimulated c-peptide post Sustacal challenge)
* Diabetes Quality of Life (DQOLY) over the first 24 months of diabetes
* Family Functioning (Family Environment Scale)over the first 24 months of diabetes

Full Information

First Posted
September 6, 2005
Last Updated
September 6, 2005
Sponsor
Children's Hospital of Eastern Ontario
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1. Study Identification

Unique Protocol Identification Number
NCT00146484
Brief Title
A Study of Two Versus Three Daily Injections in Children and Adolescents With Newly Diagnosed Type 1 Diabetes
Official Title
A Randomized Controlled Trial of Two Versus Three Daily Insulin Injections in Children and Adolescents With New Onset Type 1 Diabetes Mellitus
Study Type
Interventional

2. Study Status

Record Verification Date
September 2005
Overall Recruitment Status
Completed
Study Start Date
April 1996 (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
January 2001 (undefined)

3. Sponsor/Collaborators

Name of the Sponsor
Children's Hospital of Eastern Ontario

4. Oversight

5. Study Description

Brief Summary
The optimal insulin regimen for children and adolescents with newly diagnosed type 1 diabetes remains unknown. The purpose of this study is to determine whether a split evening injection regimen (insulin injections before breakfast, supper and bedtime) leads to better glucose control and quality of life than twice daily insulin in children and adolescents with new onset diabetes.
Detailed Description
The optimal insulin regimen for children and adolescents with newly diagnosed type 1 diabetes remains unknown. No published studies have examined the effectiveness of a split evening (three times daily) injection regimen in this group of patients. Indeed, because the first few years of diabetes management are the easiest (due to a "honeymoon" period characterised by residual insulin secretion), the potential for any benefit from more intensive management (i.e., three daily injections) may be small during this period. In addition, the intensity of the initial insulin regimen may be an important determinant of quality of life, family functioning, and subsequent compliance with diabetes regimens. A randomized controlled trial has been designed to test the hypothesis that a split evening injection regimen leads to better glycemic control and quality of life than twice daily insulin in children and adolescents with new onset diabetes.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Diabetes Mellitus, Type 1
Keywords
Diabetes Mellitus, Type 1, Child, Adolescent, Disease Management, Newly Diagnosed, Hemoglobin A, Glycosylated

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
100 (false)

8. Arms, Groups, and Interventions

Intervention Type
Drug
Intervention Name(s)
Twice Daily versus Three Times Daily Insulin Injections
Primary Outcome Measure Information:
Title
* Hemoglobin A1c over the first 24 months of diabetes
Secondary Outcome Measure Information:
Title
* Frequency of hypoglycemia (mild and severe) over the first 24 months of diabetes
Title
* Frequency of morning hyperglycemia over the first 24 months of diabetes
Title
* Residual c-peptide at two years post diagnosis (stimulated c-peptide post Sustacal challenge)
Title
* Diabetes Quality of Life (DQOLY) over the first 24 months of diabetes
Title
* Family Functioning (Family Environment Scale)over the first 24 months of diabetes

10. Eligibility

Sex
All
Maximum Age & Unit of Time
17 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: New onset type 1 diabetes Less than 48 hours since first insulin injection Child and/or parent able to read and write English Family intends to continue treatment at our institution for the next two years Informed consent from adolescents greater than 16 years of age, or if less than 16 years, informed consent from the parent/guardian with assent from the child. Exclusion Criteria: Chronic medical conditions other than treated hypothyroidism or mild asthma Concerns of the diabetes team regarding future treatment adherence making twice daily insulin preferable to the split evening injection regimen (e.g., cognitive impairment, severe family dysfunction).
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Margaret L Lawson, MD
Organizational Affiliation
Children's Hospital of Eastern Ontario
Official's Role
Principal Investigator
Facility Information:
Facility Name
Children's Hospital of Eastern Ontario
City
Ottawa
State/Province
Ontario
ZIP/Postal Code
K1H 8L1
Country
Canada

12. IPD Sharing Statement

Learn more about this trial

A Study of Two Versus Three Daily Injections in Children and Adolescents With Newly Diagnosed Type 1 Diabetes

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