The Guardcontrol Trial: Study to Assess if Type 1 Diabetics Can Improve Using the Real-time Values of Guardian RT

NCT ID: NCT00111228

Last Updated: 2019-04-01

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: NA
• Total Enrollment: 162 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2004-10-31
• Study Completion Date: 2005-05-31

Brief Summary

The objective of the study is to determine whether patients with poor glycemic control can improve metabolic control using the real-time values of the Guardian® RT compared to conventional self-monitoring blood glucose finger-sticks.

Detailed Description

Finger-stick based self-testing (SBGM), as well as diagnostic continuous glucose monitoring (CGMS®) allow diabetic patients to find a balance between the two hyper- and hypoglycemic extremes. Nevertheless, there are still patients who fail to achieve good control due to fear of hypoglycemia, or who underestimate post-prandial hyperglycemias.

The Guardian® RT Telemetered Glucose Monitoring System is indicated for continuous or periodic monitoring of real-time interstitial blood glucose values and low/high blood glucose alarms (when pre-set levels are reached) in persons with diabetes mellitus. The glucose values calculated by the device will be used to trigger hypo- and hyperglycemia alerts and will be displayed every 5 minutes. The Guardian® RT stores up to 21 days of data.

The overall primary objective of the study is to determine whether patients with poor glycemic control as evidenced by HbA1c > 8.1% can achieve improved metabolic control using the real-time values of the Guardian® RT compared to conventional self-monitoring blood glucose finger-sticks (control group) after 12 weeks of continuous use.

Conditions

Diabetes Mellitus

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Continuous use of the Guardian RT

Continuous use of the Guardian RT group

Group Type: EXPERIMENTAL

Guardian RT

Intervention Type: DEVICE

Bi-weekly use of the Guardian RT (once every 2 weeks)

Bi-weekly use of the Guardian RT (once every 2 weeks) group

Group Type: EXPERIMENTAL

Guardian RT

Intervention Type: DEVICE

Control group. SMBG monitoring

Control group. SMBG monitoring group

Group Type: ACTIVE_COMPARATOR

SMBG only

Intervention Type: DEVICE

SMBG only

Interventions

Guardian RT

Intervention Type: DEVICE

SMBG only

SMBG only

Intervention Type: DEVICE

Eligibility Criteria

Inclusion Criteria

• Patient has signed Informed consent form prior to Study Entry.
• Patients have been diagnosed with type 1 diabetes mellitus (DM) at least 12 months prior to Study Entry.
• HbA1c must be 8.1% or above at study entry day (central lab value).
• Patients must perform at least two self-monitoring blood glucose finger-sticks daily.
• Patients are on intensive insulin therapy; for multiple daily injections (MDI) patients specifically, be on a schedule of a minimum of 3 injections daily.
• Patients on intensive insulin therapy must be on continuous subcutaneous insulin infusion (CSII) or MDI at least 3 months prior to inclusion and should have been receiving diabetes care from the investigator of each centre for the 6 months prior to inclusion.
• Patients must be using only insulin analogues or rapid-acting human insulin for their meal boluses.
• Patients are willing to undergo all study procedures.
• Patients are trained on how to adapt their insulin dose to their meals and are knowledgeable concerning how to calculate and apply corrective insulin boluses post-prandially, as well as on the influence of physical activity and other life style factors on their glycemia.
• Patients are willing to participate in a Guardian® RT product training course
• Patients understand how to adjust and administer corrective treatment.

Exclusion Criteria

• Patient has hearing problems/is deaf.
• Patient has impaired vision/blindness so screen alarms cannot be recognized.
• Alcohol or drug abuse other than nicotine.
• Allergy to sensor or components of the sensor.
• Manifest psychiatric disturbances.
• Patients suffering from cancer, heart failure, kidney disease and other chronic debilitating conditions.
• Patient does not have a reliable support person.
• Patient is unwilling or unable to comply with the provisions of the protocol.
• Patient has scheduled travel on a plane in the next 3 months.
• Patient has scheduled a vacation which will occur between Visit 1 and Visit 2.
• Patient is participating in another device or drug study. Subject must have completed the follow-up phase of any previous study at least 30 days prior to enrollment in this trial. The subject may only be enrolled in this study once. Patient has already participated in the Centre Qualification Phase.

• Minimum Eligible Age: 8 Years
• Maximum Eligible Age: 60 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Medtronic Diabetes

INDUSTRY

Sponsor Role: lead

Principal Investigators

Dorothee Deiss, MD

Role: PRINCIPAL_INVESTIGATOR

Klinik für Allgemeine Charité, CVK

Locations

Hôpital Sud Francilien

Corbeil Esssonnes, , France

CH Robert Debre

Paris, , France

Klinik für Allgemeine Charité, CVK

Berlin, , Germany

Schneider Children Centre

Petah Tikva, , Israel

Universita Vita-Salute OspedaleS.Raffaele

Milan, , Italy

University Children's Hospital

Ljubljana, , Slovenia

Huddinge University Hospital

Huddinge, , Sweden

Royal Bournemouth Hospital

Bournemouth, , United Kingdom

Countries

France; Germany; Israel; Italy; Slovenia; Sweden; United Kingdom

Other Identifiers

EU 007_022004

Identifier Type: -

Identifier Source: org_study_id