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Clinical Trials/NCT03908762
NCT03908762
Unknown
N/A

Use of a Digital Therapeutic and Connected Devices to Support Insulin Titration

Amalgam Rx, Inc.1 site in 1 country40 target enrollmentJanuary 1, 2019

Overview

Phase
N/A
Intervention
Not specified
Conditions
Diabetes Mellitus, Type 2
Sponsor
Amalgam Rx, Inc.
Enrollment
40
Locations
1
Primary Endpoint
Change in A1C
Last Updated
7 years ago

Overview

Brief Summary

The principal objective of this application is to improve glycemic control of diabetic patients treated with basal insulin through use of an innovative, FDA-cleared smartphone-based insulin titration application connected to Bluetooth enabled glucose meters. iSage Rx (isageapp.com) allows providers to prescribe basal insulin treatment plans to patients and manages basal insulin doses utilizing clinically proven algorithms. In this pilot study, we hypothesize that this user-friendly application and seamless data capture will improve glycemic control (achieve HgbA1c <7%) and reduce the frequency and severity of hypoglycemia. Exploratory measures will include healthcare resource utilization and patient and provider satisfaction. The basal insulin titration algorithms used in iSage have had thousands of user-years' experience in FDA-mandated, closely supervised clinical trials, both for long-acting insulins (e.g., Lantus, Levemir) that have been available for a long time and for the newer ultra-long-acting ones (e.g., Tresiba, Toujeo). However, the effectiveness of iSage with a connected glucose meter has not been studied in a "real world" clinical environment. Broad use of such an application and connected devices will, we believe, prove to be cost-effective, favor early and appropriate prescription of insulin, reduce provider effort, shorten time to achieve glycemic goals, and simplify the transition to basal insulin therapy.

Registry
clinicaltrials.gov
Start Date
January 1, 2019
End Date
March 2020
Last Updated
7 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Amalgam Rx, Inc.
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • T2DM (WHO criteria) treated with basal insulin (glargine, detemir, degludec)
  • HgbA1c 8 or above
  • GFR \>60 ml/min within the last 12 months
  • English speaking, informed consent
  • Has an Android or iOS based compatible smartphone (iOS 9.0 or above; Android 4.4 or above)
  • Currently performs at least 3 fasting fingerstick glucose measurements/week
  • Have a PCP within the KU Health System

Exclusion Criteria

  • Diagnosis of hypoglycemic unawareness within 6 months of enrollment
  • Diagnosis of hyperglycemic hyperosmolar non-ketotic coma (HONK) or diabetic ketoacidosis (DKA) within 6 months of enrollment
  • Recent (within the last 6 months)/current use of non-topical steroids
  • Insulin requirements in excess of 1U/kg per day
  • Use of pioglitazone or another thiazolidinedione (TZD)
  • In the opinion of the provider, HgbA1c goals should adjusted above 7% due to infirmity, unstable cardiovascular disease, etc.

Outcomes

Primary Outcomes

Change in A1C

Time Frame: 3 Months

Mean and Median Change from Baseline

Secondary Outcomes

  • A1C in Target(Baseline to 3 months)
  • Rate of Hypoglycemia(Baseline to 3 months)

Study Sites (1)

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