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Effects of Pulsed Intravenous (IV) Insulin on Brittle and Uncontrolled Diabetes

Primary Purpose

Diabetes Mellitus

Status
Terminated
Phase
Phase 3
Locations
United States
Study Type
Interventional
Intervention
Pulsatile Intravenous Insulin Therapy (Humulin, Humulog, Novolog )
Sponsored by
Florida Atlantic University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Diabetes Mellitus focused on measuring Diabetes, Pulsatile intravenous insulin, Oral carbohydrate loading, Respiratory Quotients, Hypoglycemia, Hyperglycemia, Diabetes Mellitus, with complications

Eligibility Criteria

18 Years - 85 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • The researchers will include up to 300 patients both male and female between the ages of 18 and 85 diagnosed with type 1 or type 2 diabetes mellitus.
  • Self reporting or diagnosed with significant complications resulting from diabetes.
  • Taking oral agents and/or insulin for diabetic control.
  • Under an Endocrinologists supervision for their diabetes management.
  • Endocrinologist must assess and approve patient for participation in this study.
  • Ability to swallow without difficulty.
  • Ability to commit to the weekly time requirements associated with the study.

Exclusion Criteria:

  • Other causes of complications not related to diabetes.
  • Lack of intravenous access.
  • Pregnancy.
  • Alcohol abuse, drug addiction or the use of illegal drugs.
  • Positive HIV.
  • Inability to breathe into machine for respiratory quotients.

Sites / Locations

  • Florida Atlantic University

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Insulin

Arm Description

Brittle diabetic patients or patients with uncontrolled blood sugars will complete blood sugar diaries weekly and have hemoglobin A1c lab tests performed quarterly to evaluate progress in stabilizing blood sugars.

Outcomes

Primary Outcome Measures

Evaluate the effectiveness of Pulsed IV Insulin Therapy on the stabilization of blood glucose levels on patients with brittle or uncontrolled diabetes

Secondary Outcome Measures

Full Information

First Posted
August 6, 2009
Last Updated
February 2, 2016
Sponsor
Florida Atlantic University
Collaborators
Advanced Diabetes Treatment Centers
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1. Study Identification

Unique Protocol Identification Number
NCT01029444
Brief Title
Effects of Pulsed Intravenous (IV) Insulin on Brittle and Uncontrolled Diabetes
Official Title
Effects of Pulsatile Intravenous Insulin on Brittle Diabetes and Glucose Control
Study Type
Interventional

2. Study Status

Record Verification Date
February 2016
Overall Recruitment Status
Terminated
Why Stopped
Administrative
Study Start Date
March 2007 (undefined)
Primary Completion Date
March 2011 (Actual)
Study Completion Date
March 2012 (Actual)

3. Sponsor/Collaborators

Name of the Sponsor
Florida Atlantic University
Collaborators
Advanced Diabetes Treatment Centers

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The purpose of this study is to determine if restoring normal metabolic function in patients with either type I or type II diabetes can improve the impact of the consequences of diabetic complications specifically on the wide swings in blood glucoses with erratic control even under optimal conditions. Patients are treated once a week with pulsatile intravenous insulin therapy mimicking normal insulin secretion. Blood sugar diaries and laboratory tests including quarterly Hemoglobin A1c levels are monitored to measure progress and outcomes.
Detailed Description
It is known that the glucose metabolic pathway (glycolysis) is the primary fuel generator in the brain and nerve tissue, the heart and vascular tissue, the eye, the kidney and the liver Deficient metabolic states such as seen in the glucose metabolism of diabetics can lead to sequelae. These damaging effects are exacerbated by altered cellular metabolites, specifically the increase in catabolic and decrease in anabolic factors. It has been shown over the past twenty years that normalization of metabolism in diabetic patients can be accomplished by mimicking the normal endogenous insulin pattern (i.e., in pulses). Pulsatile intravenous insulin infusion has been demonstrated to stabilize the erratic wide swings in blood glucose levels and the overall stabilization of hyperglycemic and hypoglycemic events in Type 1 diabetic patients. This study was established to evaluate the effect of providing pulsatile intravenous insulin therapy on both type 1 and type 2 diabetes to determine the effect on improving diabetic control on patients with high blood glucose levels in spite of multiple insulin injections and wide swings in blood sugar despite good control. The RQ is determined by the use of a metabolic cart. Individuals breathe into a mask for 3-5 minutes after a rest period of 30 or more minutes. The ratio of exhaled volume of CO2 to the inhaled volume of O2 is determined as the RQ. The physiologic range is 0.7 to1.3. Individuals using fat as a primary fuel have a ratio of 0.7, protein or mixed fuels is 0.8-0.9 and carbohydrate is 0.9-1.0. Those taking excessive calories will have RQ's higher than 1.05. The RQ can be followed serially and this is done before and after each pulsatile IV insulin treatment, during the 3 successive sessions on a single treatment day. The amount of intravenous insulin and oral glucose given is determined by the RQ changes during the previous session.pulsatile IV insulin therapy encourages the glucose metabolism in diabetics to normalize in multiple organs, especially muscle, retina, liver, kidney and nerve endings. The process fundamentally requires the administration of high dose insulin pulses similar to those found in non diabetic humans by their pancreas into the surrounding portal circulation. Oral carbohydrates are given simultaneously to augment the process and prevent hypoglycemia. The process is monitored by frequent glucose levels and respiratory quotients (RQ). RQ is measured by a metabolic cart which determines the ratio VCO2/ VO2. This ratio is specific for the fuel used at any one time by the body. The glucose levels are monitored to keep glucose levels appropriate and the RQ determines the need to readjust the infusion protocol in each patient for subsequent insulin infusion sessions.Patient is evaluated post session and discharged when stable. Frequent monitoring of RQ is necessary as these levels change rapidly, depending on the fuel being utilized by the body. Pulsatile IV insulin therapy shifts metabolism from primarily fatty acid metabolism to primarily glucose metabolism. This shift is reflected by the increase in respiratory quotient. However during rest periods the RQ may fall back to lower levels. Therefore RQ's are done at the beginning and at the end of each insulin infusion session of 1 hour in order to appropriately monitor and adjust insulin and carbohydrate loads to reach optimal activation in each session

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Diabetes Mellitus
Keywords
Diabetes, Pulsatile intravenous insulin, Oral carbohydrate loading, Respiratory Quotients, Hypoglycemia, Hyperglycemia, Diabetes Mellitus, with complications

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
300 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Insulin
Arm Type
Experimental
Arm Description
Brittle diabetic patients or patients with uncontrolled blood sugars will complete blood sugar diaries weekly and have hemoglobin A1c lab tests performed quarterly to evaluate progress in stabilizing blood sugars.
Intervention Type
Procedure
Intervention Name(s)
Pulsatile Intravenous Insulin Therapy (Humulin, Humulog, Novolog )
Intervention Description
Patients receive weekly treatments of Pulsatile Intravenous insulin therapy. The patient's Endocrinologist determines the insulin dosage each week based upon the patient's response to treatment RQ levels and their insulin resistance.
Primary Outcome Measure Information:
Title
Evaluate the effectiveness of Pulsed IV Insulin Therapy on the stabilization of blood glucose levels on patients with brittle or uncontrolled diabetes
Time Frame
Blood sugar diaries are collected weekly and HA1c labs are collected at baseline and quarterly to assess progress

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
85 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: The researchers will include up to 300 patients both male and female between the ages of 18 and 85 diagnosed with type 1 or type 2 diabetes mellitus. Self reporting or diagnosed with significant complications resulting from diabetes. Taking oral agents and/or insulin for diabetic control. Under an Endocrinologists supervision for their diabetes management. Endocrinologist must assess and approve patient for participation in this study. Ability to swallow without difficulty. Ability to commit to the weekly time requirements associated with the study. Exclusion Criteria: Other causes of complications not related to diabetes. Lack of intravenous access. Pregnancy. Alcohol abuse, drug addiction or the use of illegal drugs. Positive HIV. Inability to breathe into machine for respiratory quotients.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Betty Tuller, PhD
Organizational Affiliation
Florida Atlantic University
Official's Role
Study Director
Facility Information:
Facility Name
Florida Atlantic University
City
Boca Raton
State/Province
Florida
ZIP/Postal Code
33421
Country
United States

12. IPD Sharing Statement

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Effects of Pulsed Intravenous (IV) Insulin on Brittle and Uncontrolled Diabetes

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