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Using Glucose Sensors to Prevent Hypoglycemia

Primary Purpose

Type 1 Diabetes, Hypoglycemia

Status
Completed
Phase
Phase 3
Locations
Canada
Study Type
Interventional
Intervention
Use of glucose sensor (Paradigm Guardian)
Sponsored by
University of Alberta
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Type 1 Diabetes focused on measuring Type 1 diabetes, Hypoglycemia, Glucose sensor

Eligibility Criteria

18 Years - 70 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Type 1 Diabetes Mellitus confirmed by C-peptide <0.10 nmol/L
  • age 18 - 70 yrs.
  • HYPO score >423
  • normal TSH, serum cortisol and anti-transglutaminase (ATTG)

Exclusion Criteria:

  • current diagnosis of cancer
  • planning a pregnancy
  • Inability to give informed consent

Sites / Locations

  • University of Alberta Hospital
  • University of Alberta

Arms of the Study

Arm 1

Arm 2

Arm Type

No Intervention

Experimental

Arm Label

A

B

Arm Description

Run in period

Outcomes

Primary Outcome Measures

Decrease in HYPO score

Secondary Outcome Measures

Number of episodes of severe hypoglycemia
Number of patients who decide to continue using the device

Full Information

First Posted
November 2, 2007
Last Updated
September 12, 2011
Sponsor
University of Alberta
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1. Study Identification

Unique Protocol Identification Number
NCT00554281
Brief Title
Using Glucose Sensors to Prevent Hypoglycemia
Official Title
Paradigm Real Time Continuous Glucose Monitoring Device for the Prevention of Hypoglycemia
Study Type
Interventional

2. Study Status

Record Verification Date
September 2011
Overall Recruitment Status
Completed
Study Start Date
October 2006 (undefined)
Primary Completion Date
August 2008 (Actual)
Study Completion Date
August 2008 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Alberta

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Hypoglycemia is the most common complication of Type 1 diabetes particularly in those who strive for good glycemic control. In some patients there is a loss of awareness of hypoglycaemia so that the first manifestation of hypoglycaemia may be confusion or coma. Such a situation may carry risks that the patient may harm him or her self. Medtronic has recently developed a continuous glucose sensor that determines the glucose level every 3 minutes using a subcutaneous sensor and transmits the information to a remote device (Paradigm RT) that may be worn or left close by eg on a bedside table. The device may be programmed to alarm for a rapidly falling glucose or for low glucose levels. We propose to use this in 16 patients with severe hypoglycemia as evidenced by a high HYPO score and see if we can decrease the number of hypoglycemic reactions and document this improvement with a better HYPO score.
Detailed Description
Sixteen patients with Type 1 diabetes (as defined by: onset under the age of 25, lean at time of onset, continuous insulin use, and/or history of ketoacidosis and C-peptide negative), with a HYPO score over the seventy-fifth percentile (>423), will be approached and offered the study. The study will be conducted over a three month time-frame. The first month will be a run-in period for participants to collect four weeks of glucose readings and information about their hypoglycemic events. These records will be used to calculate the baseline modified HYPO score. Patients will be screened during the first month for thyroid disease, celiac disease and Addison's disease. During the second month they will meet with the study nurse for an intensive instruction period on the use of the Paradigm RT sensor. They will spend this month practicing to use the sensor and confirming they can use it adequately. During the final month they will wear the sensor and collect glucose and hypoglycemia records for calculation of the final modified HYPO score. The end point will be the change from the baseline modified HYPO score to the final four week HYPO score and this would be used to identify any improvement.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Type 1 Diabetes, Hypoglycemia
Keywords
Type 1 diabetes, Hypoglycemia, Glucose sensor

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
16 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
A
Arm Type
No Intervention
Arm Description
Run in period
Arm Title
B
Arm Type
Experimental
Intervention Type
Device
Intervention Name(s)
Use of glucose sensor (Paradigm Guardian)
Other Intervention Name(s)
Paradigm Guardian glucose sensor
Intervention Description
Use glucose sensor to prevent episodes of severe hypoglycemia
Primary Outcome Measure Information:
Title
Decrease in HYPO score
Time Frame
3 months
Secondary Outcome Measure Information:
Title
Number of episodes of severe hypoglycemia
Time Frame
3 months
Title
Number of patients who decide to continue using the device
Time Frame
3 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Type 1 Diabetes Mellitus confirmed by C-peptide <0.10 nmol/L age 18 - 70 yrs. HYPO score >423 normal TSH, serum cortisol and anti-transglutaminase (ATTG) Exclusion Criteria: current diagnosis of cancer planning a pregnancy Inability to give informed consent
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Edmond A Ryan, MD
Organizational Affiliation
University of Alberta
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Alberta Hospital
City
Edmonton
State/Province
Alberta
ZIP/Postal Code
T6G 2B7
Country
Canada
Facility Name
University of Alberta
City
Edmonton
State/Province
Alberta
ZIP/Postal Code
T6G 2S2
Country
Canada

12. IPD Sharing Statement

Citations:
PubMed Identifier
19821755
Citation
Ryan EA, Germsheid J. Use of continuous glucose monitoring system in the management of severe hypoglycemia. Diabetes Technol Ther. 2009 Oct;11(10):635-9. doi: 10.1089/dia.2009.0042.
Results Reference
result

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Using Glucose Sensors to Prevent Hypoglycemia

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