Feasibility Study of an Integrated Sensor and Infusion Set

NCT ID: NCT01770561

Last Updated: 2013-02-05

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: NA
• Total Enrollment: 20 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2012-10-31
• Study Completion Date: 2012-10-31

Brief Summary

The purpose of this study is to collect performance data on the integrated sensor and infusion set during 3 days of use and demonstrate performance adequacy of the Integrated sensor and infusion set with glucose sensing and insulin delivery functionalities. The hypothesis of this study is that having the infusion of insulin in close proximity to the sensor does not interfere with the sensor accuracy.

Detailed Description

Sensor clinical accuracy will be evaluated based on the following parameters: Mean ARD (absolute relative difference), median ARD, Clarke Grid Analysis. Meter BG values will be used as reference. Descriptive statistics will be used to assess non-inferiority of the Integrated sensor and infusion sets sensors compare to control Enlite sensors.

Insulin delivery functionality will be evaluated based on BG profiles obtained during peri-prandial periods during which BG measurements will be performed at 15, 20, 30 min intervals according to a SMBG schedule. Post-prandial pharmacodynamic profiles will be analyzed to demonstrate the effect of insulin delivered using the Integrated sensor and infusion set. Specifically, rise in glucose levels followed by their fall will be used as an indication that insulin was delivered and absorbed. Post-prandial BG areas under the curve (AUC), Tmax (time to maximum rise of BG), and Cmax (maximum post-prandial BG) values will be calculated for each meal (breakfast, lunch, and dinner) consumed during both inpatient days and compared. Intra - and inter-subject mean values and standard deviations will be calculated. Paired and unpaired T-tests will be used to evaluate statistical significance.

Longevity of device performance will be assessed by comparing the listed parameters obtained during two inpatient days.

Conditions

Diabetes Type 1

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: BASIC_SCIENCE
• Blinding Strategy: NONE

Study Groups

Integrated sensor and infusion set.

All subjects must have been previously diagnosed Type 1 Diabetics and being used to sensor augumented pumps

Group Type: EXPERIMENTAL

Integrated sensor and infusion set.

Intervention Type: DEVICE

Change patients from current devices to the Integrated sensor and infusion set.

Interventions

Integrated sensor and infusion set.

Change patients from current devices to the Integrated sensor and infusion set.

Intervention Type: DEVICE

Eligibility Criteria

Inclusion Criteria

1. Subject is 21-70 years of age at time of screening

2. Subject has a clinical diagnose of type 1 diabetes, as determined by investigator

3. Subject has one or more established insulin-to-carbohydrate ratios

4. Subject has one or more established insulin correction ratios

5. Subject is currently using a Medtronic insulin pump and has been so for a minimum of 3 months at time of enrollment.

6. Subject has been using insulin for more than one year.

7. Subject is willing to wear two pumps, one sensor, one infusion set and one Integrated sensor and infusion set at one time (first night).

8. Subject is willing to perform frequent SMBGs during Visits 3 and 4.

9. Subject is in good general health without other acute or chronic illnesses

Exclusion Criteria

1. Subject is pregnant or lactating (if female), as self-declared by patient

2. Subject plans to become pregnant during the course of the study

3. Subject is unable to tolerate tape adhesive in the area of sensor placement

4. Subject has any unresolved adverse skin condition in the area of sensor or device placement (e.g. psoriasis, rash, Staphylococcus infection)

5. The subject has complications such as advanced autonomic neuropathy, legal blindness, or symptomatic cardiovascular disease as evidenced by a cardiovascular episode within the last six months.

6. The subject has any major concomitant disease or any physical or psychological disorder within the last five years, which might be considered life threatening or which might confound the collection or interpretation of the study data.

7. The subject has experienced two or more severe hypoglycemic events - seizures/coma requiring assistance in the past 6 months.

• Minimum Eligible Age: 21 Years
• Maximum Eligible Age: 70 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Medtronic Diabetes R&D Denmark

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Kirsten Noergaard, MDD

Role: PRINCIPAL_INVESTIGATOR

Hvidovre University Hospital

Locations

Hvidovre Hospital

Hvidovre, Hvidovre, Denmark

Countries

Denmark

Other Identifiers

CER269

Identifier Type: -

Identifier Source: org_study_id