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

Diabetes Mellitus Clinical Trial

Official title:

Randomised, Controlled, Multi-centric, Clinical Study to Assess Whether Type 1 Diabetic Patients in Poor Glycemic Control Can Improve Using the Real-time Values of Guardian T Versus Conventional Self-Monitoring Blood Glucose

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT00111228
• Other study ID #: EU 007_022004
• Status: Completed
• Phase: N/A
• Start date: October 2004
• Est. completion date: May 2005

Study information

• Verified date: January 2019
• Source: Medtronic Diabetes
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial 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.

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.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 162
• Est. completion date: May 2005
• Est. primary completion date: May 2005
• Accepts healthy volunteers: No
• Gender: All
• Age group: 8 Years to 60 Years

Eligibility

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.

Related Conditions & MeSH terms

• Diabetes Mellitus

Intervention

Device:
• Guardian RT

• SMBG only
SMBG only

Locations

Country	Name	City	State
France	Hôpital Sud Francilien	Corbeil Esssonnes
France	CH Robert Debre	Paris
Germany	Klinik für Allgemeine Charité, CVK	Berlin
Israel	Schneider Children Centre	Petah Tikva
Italy	Universita Vita-Salute OspedaleS.Raffaele	Milano
Slovenia	University Children's Hospital	Ljubljana
Sweden	Huddinge University Hospital	Huddinge
United Kingdom	Royal Bournemouth Hospital	Bournemouth

Sponsors (1)

Lead Sponsor	Collaborator
Medtronic Diabetes

Countries where clinical trial is conducted

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

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Hemoglobin A1c (HbA1c) - Change From Baseline to End of 3 Month Study Period	Hemoglobin A1c (HbA1c) - change from baseline to end of 3 month study period, calculated as A1c at 3 month - A1c at baseline	baseline and 3 month after study
Secondary	Average Blood Glucose - Change From Baseline to End of 3 Month Study Period, Calculated as Average Blood Glucose at 3 Month - Average Blood Glucose at Baseline	Average blood glucose - change from baseline to end of 3 month study period, calculated as average blood glucose at 3 month - average blood glucose at baseline	baseline and 3 month after study