Observational Study to Evaluate the Effectiveness and Safety of the Dexcom G4 Continuous Glucose Monitoring System in Pediatrics

Diabetes Mellitus Clinical Trial

Official title:

Observational Study to Evaluate the Effectiveness and Safety of the Dexcom G4

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT02363907
• Other study ID #: PTL-900982
• Status: Completed
• Phase: N/A
• First received: February 10, 2015
• Last updated: July 25, 2017
• Start date: September 2012
• Est. completion date: October 2012

Study information

• Verified date: February 2015
• Source: DexCom, Inc.
• Contact: n/a
• Is FDA regulated: No
• Study type: Observational

Clinical Trial Summary

The purpose of this study is to evaluate the effectiveness and safety of the Dexcom G4 System when used as an adjuvant to blood glucose testing over a 7-day period in people 2 to 17 years-old with diabetes mellitus.

Description:

Performance of the system will be primarily evaluated by comparing the blood glucose measurements from the reference device, a blood glucose meter, to the CGM System values collected during the study. Specifically, performance will be primarily evaluated in terms of the proportion of G4 System values that are within ±20% of glucose meter reference value for glucose levels >80 mg/dL and ±20 mg/dL of glucose meter reference values <80 mg/dL. These G4-meter matched pairs will be analyzed across the 7 days of wear.

Safety data of the CGM System will also be collected and safety will be characterized by the incidence of anticipated device-related adverse events (ADEs) of subjects who participate in the study.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 30
• Est. completion date: October 2012
• Est. primary completion date: October 2012
• Accepts healthy volunteers: No
• Gender: All
• Age group: 2 Years to 17 Years

Eligibility

Inclusion Criteria:

• Ages 2 to 17 years;

• Diagnosis of diabetes mellitus;

• Treatment of diabetes with insulin and/or oral diabetes medication Note: Insulin-using subjects only - willing to avoid insulin injections or wear an insulin pump insertion set within 3 inches from the sensor site;

• Willing to refrain from the use of medications containing acetaminophen during the sensor insertion period and for one day prior to sensor insertion;

• Able to perform up to 7 fingersticks per day during home use (approximately 2 calibration fingersticks or as often as prompted by the device and approximately 5 for diabetes management and/or detection of hyper and hypoglycemia); and

• Subject or guardian is able to speak, read, and write English.

Exclusion Criteria:

• Extensive skin changes/diseases that preclude wearing the required number of devices on normal skin (e.g. extensive psoriasis, recent burns or severe sunburn, extensive eczema, extensive scarring, extensive tattoos, dermatitis herpetiformis) at the proposed wear sites;

• Known allergy to medical-grade adhesives;

• For subjects of childbearing potential: are pregnant as demonstrated by a positive pregnancy test within 72 hours prior to device insertion;

• Hematocrit value outside the range of the blood glucose monitoring system used in the study;

• Current participation in another investigational study protocol (if a subject has recently completed participation in another drug study, the subject must have completed that study at least 30 days prior to being enrolled in this study);

• Planned MRI scan, CT scan, or diathermy during the week of the study; or

• Any condition that, in the opinion of the Investigator, would interfere with their participation in the trial (e.g., marked visual impairment) or pose an excessive risk to study staff handling venous blood samples (e.g., known history of hepatitis B or C, or HIV).

Related Conditions & MeSH terms

• Diabetes Mellitus

Locations

Country	Name	City	State
United States	Rocky Mountain Diabetes and Osteoporosis Center	Idaho Falls	Idaho

Sponsors (1)

Lead Sponsor	Collaborator
DexCom, Inc.

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Point Accuracy of CGM ISF Readings to Blood Glucose Measured by a Reference Device	"Point Accuracy was evaluated in terms of the percentage of CGM values that were within ±20% of glucose meter reference value for glucose levels >80 mg/dL and ±20 mg/dL of glucose meter reference values for glucose levels <80 mg/dL	Measured during clinic session during 7 day sensor wear period