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Completed

NCT Number: NCT00357890

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

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).

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Key information

Age range

12 year–17 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Nemours Children's Clinic

Jacksonville, Florida, 32207, United States

About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

Insulin pump therapy

Device

CSII initiated within 1 month of diagnosis

Other names: Continuous subcutaneous insulin infusion (CSII)

Multiple daily injections using insulin glargine + rapid acting analog

Drug

MDI as control

Other names: MDI using glargine plus a rapid acting analog

Primary outcomes

  1. Insulin Sensitivity

    Time frame: 24 months

    Insulin sensitivity - glucose infusion rate (GIR) obtained from hyperinsulinemic-euglycemic clamp. Higher GIR reflects higher insulin sensitivity, lower GIR reflects lower insulin sensitivity.

  2. Beta Cell Function

    Time frame: 24 months

    Beta cell function as assessed by peak c-peptide using mixed meal tolerance testing

Secondary outcomes

  1. Hemoglobin A1c

    Time frame: 24 months

    Hemoglobin A1c (HbA1c) (%)

  2. Percent Body Fat

    Time frame: 24 months

    Percent body fat based on DEXA scan (%BF)

Sponsors and collaborators

Lead sponsor

Nemours Children's Clinic

Other

Registry information

Official study 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.

Important dates

Study start
2005
Primary completion
2014
Study completion
2014
First posted
Jul 28, 2006
Registry last updated
Jul 7, 2023

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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