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Glucose Variability in Subclinical Hypertrophy

Primary Purpose

Diabetes Mellitus, Lipohypertrophy

Status
Active
Phase
Not Applicable
Locations
Canada
Study Type
Interventional
Intervention
Lipohypertrophy
Normal Subcutaneous Tissue
Sponsored by
University of British Columbia
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional other trial for Diabetes Mellitus focused on measuring iPro2 Continuous Blood Glucose Recorder, Subclinical

Eligibility Criteria

19 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Participation in phase 1
  • Type 1 or Type 2 diabetes for at least 2 years
  • Using insulin to manage diabetes
  • At least 19 years of age

Exclusion Criteria:

  • Taking insulin secretagogues (gliclazide, glyburide, glipizide
  • Taking other injectable diabetes medications (i.e. liraglutide, Victoza)
  • Taking systemic steroids (e.g. prednisone)
  • Not fluent in speaking and writing English (unless accompanied by a translator)

Sites / Locations

  • Gerontology Research Lab
  • Vancouver General Hospital Diabetes Centre

Arms of the Study

Arm 1

Arm 2

Arm Type

Other

Other

Arm Label

Lipohypertrophy

Normal Subcutaneous Tissue

Arm Description

Participants inject their insulin into the abdomen into areas of lipohypertrophy that were identified by ultrasound in Phase 1 of the study.

Participants inject their insulin into the abdomen into areas with normal subcutaneous tissue.

Outcomes

Primary Outcome Measures

Blood glucose levels
iPro2 Continuous Blood Glucose Monitor

Secondary Outcome Measures

Full Information

First Posted
April 20, 2016
Last Updated
May 8, 2023
Sponsor
University of British Columbia
Collaborators
Medtronic
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1. Study Identification

Unique Protocol Identification Number
NCT02748434
Brief Title
Glucose Variability in Subclinical Hypertrophy
Official Title
Glucose Variability in Subclinical Hypertrophy
Study Type
Interventional

2. Study Status

Record Verification Date
May 2023
Overall Recruitment Status
Active, not recruiting
Study Start Date
October 2016 (Actual)
Primary Completion Date
December 2023 (Anticipated)
Study Completion Date
May 1, 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of British Columbia
Collaborators
Medtronic

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Evaluation of insulin absorption at sites affected by clinically apparent lipohypertrophy through short-term continuous glucose monitoring has shown inconsistent results and it is yet unknown how or if subclinical lipohypertrophy affects absorption. In this study investigators propose to enroll at least 20 people who participated in phase 1 and who were determined to have subclinical lipohypertrophy to examine the correlation between glycemic control and amount of insulin injected in subclinical hypertrophic areas using capillary blood glucose and continuous glucose monitoring.
Detailed Description
Patients will be randomized and data interpreters will be blinded to two alternating six-day protocols where the patients will be advised verbally and by written instruction to inject insulin in sites of subclinical lipohypertrophy or normal subcutaneous tissue. Patients will be asked to monitor and record their capillary blood glucose with meals and prior to bedtime using their own capillary blood glucose monitor. A trained research nurse at the Diabetes Centre will instrument each patient with an iPro 2 glucose sensor (Medtronic Canada). These sensors continuously measure blood glucose for periods of up to 7 days. A trained nurse will clean the skin with a superficial disinfectant and a small catheter will be inserted in the subcutaneous tissue at a non-lipohypertrophic site. The catheter will then be attached to a glucose sensor. Patients will wear this sensor for two periods of 6 days each at different sites. At the end of each of the two six day periods, the sensor will be removed.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Diabetes Mellitus, Lipohypertrophy
Keywords
iPro2 Continuous Blood Glucose Recorder, Subclinical

7. Study Design

Primary Purpose
Other
Study Phase
Not Applicable
Interventional Study Model
Crossover Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
9 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Lipohypertrophy
Arm Type
Other
Arm Description
Participants inject their insulin into the abdomen into areas of lipohypertrophy that were identified by ultrasound in Phase 1 of the study.
Arm Title
Normal Subcutaneous Tissue
Arm Type
Other
Arm Description
Participants inject their insulin into the abdomen into areas with normal subcutaneous tissue.
Intervention Type
Other
Intervention Name(s)
Lipohypertrophy
Intervention Type
Other
Intervention Name(s)
Normal Subcutaneous Tissue
Primary Outcome Measure Information:
Title
Blood glucose levels
Description
iPro2 Continuous Blood Glucose Monitor
Time Frame
Continuously for 12 days

10. Eligibility

Sex
All
Minimum Age & Unit of Time
19 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Participation in phase 1 Type 1 or Type 2 diabetes for at least 2 years Using insulin to manage diabetes At least 19 years of age Exclusion Criteria: Taking insulin secretagogues (gliclazide, glyburide, glipizide Taking other injectable diabetes medications (i.e. liraglutide, Victoza) Taking systemic steroids (e.g. prednisone) Not fluent in speaking and writing English (unless accompanied by a translator)
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Graydon Meneilly, MD
Organizational Affiliation
University of British Columbia
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Jordanna Kapeluto, MD
Organizational Affiliation
University of British Columbia
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Breay Paty, MD
Organizational Affiliation
University of British Columbia
Official's Role
Principal Investigator
Facility Information:
Facility Name
Gerontology Research Lab
City
Vancouver
State/Province
British Columbia
ZIP/Postal Code
V5Z 1M9
Country
Canada
Facility Name
Vancouver General Hospital Diabetes Centre
City
Vancouver
State/Province
British Columbia
ZIP/Postal Code
V5Z 1M9
Country
Canada

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

Glucose Variability in Subclinical Hypertrophy

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