Can Continuous Glucose Measurements Help Diabetic Patients Treated With an Implantated Pump? (CGMIP)

University Hospital Center (CHU)

Status

Terminated

Conditions

Type1diabetes

Treatments

Device: Continuous Glucose Measurement (CGM)

Study type

Interventional

Funder types

Other

Identifiers

NCT03048227

UF9773

Details and patient eligibility

About

During this study, we propose to assess the utility of Continuous Glucose Measurements (CGM) in a group of Type 1 diabetic patients treated with an implanted insulin pump. Patients will participate in two period of 3 months separated by a 3 months washout. During one period, they will use CGM to adapt their insulin therapy while during the other period, they will manage their diabetes with their usual capillary blood glucose meter. We except to observe an increase of time spent in glucose safe range when using CGM.

Full description

Glucose control and quality of life of patients with type 1 diabetes with high glucose variability can be improve with use of an implanted pump which delivers insulin by the intra-peritoneal route. Some patients however still have difficulties to achieve their glycemic goal despite this therapy. Continuous Glucose Measurements (CGM) has proven to be able to improve glucose control (HbA1c, time spent in hypoglycaemia) of patients treated with an external insulin pump. No trial has been performed yet to assess the utility of CGM on patients using an intra-peritoneal insulin delivery.

During this study, we propose to assess the influence of CGM use on type 1 diabetic subject treated with implanted insulin pump. It is a prospective, randomized cross-over study. After a 2 weeks run-in period with CGM followed by a 4 weeks break, subjects will participate at two experimental periods of 3 months separated with a 3 month washout. During the intervention phase, patient will use a CGM system (Abbott Freestyle Navigator II) to adapt their insulinotherapy. During the control period, patients will based their insulinotherapy upon their usual care and capillary glucose measurements. The order of the periods will be randomized.

The main endpoint will be the time spent in glucose interval 70-180mg/dL during the last 20 days of each period. The control arm will wear a blinded sensor during this phase to allow comparison.

Enrollment

15 patients

Sex

All

Ages

18 to 70 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Age from 18 and 70
Type 1 diabetes for at least 1 year
Treatment of diabetes withimplanted insulin pump for at least 6 months
HbA1c level between 7.5 and 10%
Minimum of 4 capillary glucose controls per day over past 3 months
Use of CGM at least 75% during run-in period
Willingness to follow all study procedures
Informed consent signed
Patient must be affiliated or beneficiary of a social medical insurance

Exclusion criteria

Pregnancy of breast feeding, or intention to be pregnant during the study duration
Impaired cognitive or psychological abilities which may result in defective adherence to study procedures
Any disease which could make the use glucose sensor difficult (ex : blindness, severe arthrosis or immobility)
Known allergy to medical adhesive or glucose sensor component
Medication affecting glucose metabolism, unless stable during the study
Long term use of continuous glucose measurements during pas 6 months
Pump implanted more than 6 years ago
Anti-insulin antobodies syndrom
Active enrollment in another clinical trial or participation in a study within 30 days