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Diabetes Technol Ther. 2018 Mar;20(3):197-206. doi: 10.1089/dia.2017.0142. Epub 2018 Jan 30.

A Prospective Multicenter Evaluation of the Accuracy of a Novel Implanted Continuous Glucose Sensor: PRECISE II.

Author information

1
1 Diablo Clinical Research , Walnut Creek, California.
2
2 Rainier Clinical Research Center, Inc. , Renton, Washington.
3
3 John Muir Physician Network Clinical Research Center , Concord, California.
4
4 Department of Medicine, Mount Sinai Diabetes Center , New York, New York.
5
5 Clinical Trials of Texas, Inc. , San Antonio, Texas.
6
6 Worldwide Clinical Trials , San Antonio, Texas.
7
7 Atlanta Diabetes Associates , Atlanta, Georgia .
8
8 Clinical Sciences and Medical Affairs, Senseonics, Inc. , Germantown, Maryland.
9
9 AMCR Institute, Inc. , Escondido, California.

Abstract

BACKGROUND:

Persistent use of real-time continuous glucose monitoring (CGM) improves diabetes control in individuals with type 1 diabetes (T1D) and type 2 diabetes (T2D).

METHODS:

PRECISE II was a nonrandomized, blinded, prospective, single-arm, multicenter study that evaluated the accuracy and safety of the implantable Eversense CGM system among adult participants with T1D and T2D (NCT02647905). The primary endpoint was the mean absolute relative difference (MARD) between paired Eversense and Yellow Springs Instrument (YSI) reference measurements through 90 days postinsertion for reference glucose values from 40 to 400 mg/dL. Additional endpoints included Clarke Error Grid analysis and sensor longevity. The primary safety endpoint was the incidence of device-related or sensor insertion/removal procedure-related serious adverse events (SAEs) through 90 days postinsertion.

RESULTS:

Ninety participants received the CGM system. The overall MARD value against reference glucose values was 8.8% (95% confidence interval: 8.1%-9.3%), which was significantly lower than the prespecified 20% performance goal for accuracy (P < 0.0001). Ninety-three percent of CGM values were within 20/20% of reference values over the total glucose range of 40-400 mg/dL. Clarke Error Grid analysis showed 99.3% of samples in the clinically acceptable error zones A (92.8%) and B (6.5%). Ninety-one percent of sensors were functional through day 90. One related SAE (1.1%) occurred during the study for removal of a sensor.

CONCLUSIONS:

The PRECISE II trial demonstrated that the Eversense CGM system provided accurate glucose readings through the intended 90-day sensor life with a favorable safety profile.

KEYWORDS:

Accuracy; Continuous glucose monitoring; Implantable; Longevity; Type 1 diabetes; Type 2 diabetes

PMID:
29381090
PMCID:
PMC5867508
DOI:
10.1089/dia.2017.0142
[Indexed for MEDLINE]
Free PMC Article

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