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Early Administration of Long-acting Insulin Treatment of Diabetic Ketoacidosis in Pediatric Type 1 Diabetes

Primary Purpose

Diabetes Mellitus, Type 1, Diabetic Ketoacidosis

Status
Terminated
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Glargine
IV insulin
Electrolyte Correction
Correction of Fluid Loss
Sponsored by
Chattanooga-Hamilton County Hospital Authority
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Diabetes Mellitus, Type 1

Eligibility Criteria

1 Year - 21 Years (Child, Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • T1DM
  • Hyperglycemia >200 mg/dl
  • Bicarbonate ≤ 15 mmol/L
  • pH < 7.3
  • Ketonemia
  • Ketonuria
  • Glucosuria
  • Admission to PICU (Pediatric Intensive Care Unit)
  • Ages 1-21 years

Exclusion Criteria:

  • Patients who received glargine within the last 24 hours
  • Patients with sepsis

Sites / Locations

  • Children's @ Erlanger

Arms of the Study

Arm 1

Arm 2

Arm Type

Placebo Comparator

Experimental

Arm Label

Control Group

Treatment Group

Arm Description

The control group will receive all traditional methods of treatment for DKA including iv insulin, correction of fluid loss, and electrolyte correction, including a placebo subcutaneous injection.

The study group will receive the same treatment including iv insulin, correction of fluid loss, and electrolyte correction, but will be supplemented with a subcutaneous glargine injection.

Outcomes

Primary Outcome Measures

Blood glucose

Secondary Outcome Measures

Blood glucose
checking for changes in levels after intervention initiation
blood pH
blood pH
checking for changes in levels after intervention initiation
blood bicarbonate level
blood bicarbonate level
checking for changes in levels after intervention initiation
Urinalysis for levels of ketones & glucosuria
Urinalysis for levels of ketones & glucosuria
checking for changes in levels after intervention initiation

Full Information

First Posted
September 9, 2015
Last Updated
September 21, 2020
Sponsor
Chattanooga-Hamilton County Hospital Authority
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1. Study Identification

Unique Protocol Identification Number
NCT02548494
Brief Title
Early Administration of Long-acting Insulin Treatment of Diabetic Ketoacidosis in Pediatric Type 1 Diabetes
Official Title
Early Administration of Long-acting Insulin Glargine for the Treatment of Diabetic Ketoacidosis in Pediatric Type 1 Diabetes: A Randomized Double Blind Trial
Study Type
Interventional

2. Study Status

Record Verification Date
September 2020
Overall Recruitment Status
Terminated
Why Stopped
Project terminated due to insufficient resources for recruitment.
Study Start Date
November 2015 (undefined)
Primary Completion Date
February 1, 2019 (Actual)
Study Completion Date
February 1, 2019 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Chattanooga-Hamilton County Hospital Authority

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The management goals of diabetic ketoacidosis (DKA) in the pediatric type 1 diabetes (T1DM) population are fluid and electrolyte repletion, insulin administration, and correction of acidosis in order to stabilize the patient. Traditionally, a rapid-acting insulin IV infusion is begun immediately and continued until the acidosis is corrected and hyperglycemia normalized. Once the acidosis is corrected, patients are able to be transitioned to a subcutaneous insulin regimen. The role that a subcutaneous long-acting insulin such as glargine has in the acute treatment of DKA has not been extensively studied. While giving glargine during the treatment of DKA is becoming more common place, few studies have examined the potential risks and benefits of its use. This study will investigate the effects of early administration of glargine during DKA in patients with newly diagnosed TIDM. The design of this study is a prospective, double-blind study of children ages 2-21 who are admitted to the hospital in DKA with a diagnosis of T1DM. The control group will receive all traditional methods of treatment for DKA, including a placebo subcutaneous injection. The study group will receive the same treatment, but will be supplemented with a subcutaneous glargine injection.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Diabetes Mellitus, Type 1, Diabetic Ketoacidosis

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigator
Allocation
Randomized
Enrollment
17 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Control Group
Arm Type
Placebo Comparator
Arm Description
The control group will receive all traditional methods of treatment for DKA including iv insulin, correction of fluid loss, and electrolyte correction, including a placebo subcutaneous injection.
Arm Title
Treatment Group
Arm Type
Experimental
Arm Description
The study group will receive the same treatment including iv insulin, correction of fluid loss, and electrolyte correction, but will be supplemented with a subcutaneous glargine injection.
Intervention Type
Drug
Intervention Name(s)
Glargine
Other Intervention Name(s)
Lantus
Intervention Description
The control group will receive all traditional methods of treatment for DKA, including a placebo subcutaneous injection. The study group will receive the same treatment, but will be supplemented with a subcutaneous glargine injection.
Intervention Type
Drug
Intervention Name(s)
IV insulin
Intervention Description
The intravenous infusion of insulin at a weight-based fixed rate until ketosis has subsided.
Intervention Type
Other
Intervention Name(s)
Electrolyte Correction
Intervention Description
If the potassium level is greater than 6 mEq/L, do not administer potassium supplement. If the potassium level is 4.5-6 mEq/L, administer 10 mEq/h of potassium chloride. If the potassium level is 3-4.5 mEq/L, administer 20 mEq/h of potassium chloride.
Intervention Type
Other
Intervention Name(s)
Correction of Fluid Loss
Intervention Description
Initial correction of fluid loss is either by isotonic sodium chloride solution or by lactated Ringer solution. The recommended schedule for restoring fluids is as follows: Administer 1-3 L during the first hour. Administer 1 L during the second hour. Administer 1 L during the following 2 hours Administer 1 L every 4 hours, depending on the degree of dehydration and central venous pressure readings
Primary Outcome Measure Information:
Title
Blood glucose
Time Frame
Within 3 hrs of arrival
Secondary Outcome Measure Information:
Title
Blood glucose
Description
checking for changes in levels after intervention initiation
Time Frame
4 hours after intervention initiation
Title
blood pH
Time Frame
within 3 hours of arrival
Title
blood pH
Description
checking for changes in levels after intervention initiation
Time Frame
4 hours after intervention initiation
Title
blood bicarbonate level
Time Frame
Within 3 hrs of arrival
Title
blood bicarbonate level
Description
checking for changes in levels after intervention initiation
Time Frame
4 hours after intervention initiation
Title
Urinalysis for levels of ketones & glucosuria
Time Frame
Within 3 hrs of arrival
Title
Urinalysis for levels of ketones & glucosuria
Description
checking for changes in levels after intervention initiation
Time Frame
4 hours after intervention initiation
Other Pre-specified Outcome Measures:
Title
Length of PICU Stay
Time Frame
1-2 days
Title
Length of Hospital Stay
Time Frame
1-5 days
Title
Hypoglycemic events
Description
Hypoglycemia is defined as blood glucose less than 70 mg/dL.
Time Frame
length of hospital stay, an expected average of 3 days

10. Eligibility

Sex
All
Minimum Age & Unit of Time
1 Year
Maximum Age & Unit of Time
21 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: T1DM Hyperglycemia >200 mg/dl Bicarbonate ≤ 15 mmol/L pH < 7.3 Ketonemia Ketonuria Glucosuria Admission to PICU (Pediatric Intensive Care Unit) Ages 1-21 years Exclusion Criteria: Patients who received glargine within the last 24 hours Patients with sepsis
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Rita Shridharani, MD
Organizational Affiliation
UTCOMC/ Children's at Erlanger
Official's Role
Principal Investigator
Facility Information:
Facility Name
Children's @ Erlanger
City
Chattanooga
State/Province
Tennessee
ZIP/Postal Code
37403
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
Undecided
Citations:
Citation
Levitsky LL et al. Epidemiology, presentation, and diagnosis of type 1 diabetes mellitus in children and adolescents. In: UpToDate, Wolfsdorf J (Ed), UpToDate, Waltham, MA. (Accessed on November 3, 2014.)
Results Reference
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Citation
Jeha GS, Haymond Mw. Treatment and complications of diabetic ketoacidosis in children. In: UpToDate, Waltham MA. (Accessed on November 4, 2014.)
Results Reference
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PubMed Identifier
24840321
Citation
Urakami T, Naito Y, Seino Y. Insulin glargine in pediatric patients with type 1 diabetes in Japan. Pediatr Int. 2014 Dec;56(6):822-828. doi: 10.1111/ped.12379. Epub 2014 Sep 16.
Results Reference
background
PubMed Identifier
17508198
Citation
Shankar V, Haque A, Churchwell KB, Russell W. Insulin glargine supplementation during early management phase of diabetic ketoacidosis in children. Intensive Care Med. 2007 Jul;33(7):1173-1178. doi: 10.1007/s00134-007-0674-3. Epub 2007 May 17.
Results Reference
background
PubMed Identifier
22685233
Citation
Hsia E, Seggelke S, Gibbs J, Hawkins RM, Cohlmia E, Rasouli N, Wang C, Kam I, Draznin B. Subcutaneous administration of glargine to diabetic patients receiving insulin infusion prevents rebound hyperglycemia. J Clin Endocrinol Metab. 2012 Sep;97(9):3132-7. doi: 10.1210/jc.2012-1244. Epub 2012 Jun 8.
Results Reference
background
Citation
6Lexicomp online
Results Reference
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Early Administration of Long-acting Insulin Treatment of Diabetic Ketoacidosis in Pediatric Type 1 Diabetes

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