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NCT03207893

Benefits of Continuous Glucose Monitoring With GEM Lifestyle Modification for Adults With Type 2 Diabetes

Completed NA Last updated 26 February 2021
What this trial tests

NA trial testing GEM lifestyle modification & continuous glucose monitoring in Diabetes Mellitus, Type 2 in 24 participants. Completed in 23 January 2020.

Timeline
19 July 2018
Primary endpoint
23 January 2020
23 January 2020

Quick facts

Lead sponsorUniversity of Virginia
PhaseNA
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingnone
Primary purposetreatment
Enrollment24
Start date19 July 2018
Primary completion23 January 2020
Estimated completion23 January 2020
Sites1 location across United States

Drugs / interventions tested

Conditions studied

Sponsor

University of Virginia

Who can join

Adults 21 to 80, any sex, with Diabetes Mellitus, Type 2. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The purpose of this study is to determine if the use of continuous glucose monitoring with the GEM lifestyle modification program (Glycemic load, Exercise and Monitoring glucose) will result in better diabetes control than routine care.

Publications & conference data

1 peer-reviewed publication reference this trial (live from Europe PMC):

  1. Minimizing Glucose Excursions (GEM) With Continuous Glucose Monitoring in Type 2 Diabetes: A Randomized Clinical Trial.
    Cox DJ, Banton T, Moncrief M, Conaway M, et al · · 2020 · cited 54× · PMID 33094208 · DOI 10.1210/jendso/bvaa118

Verify or expand the search:

Other recruiting trials for Diabetes Mellitus, Type 2

Currently open trials in the same condition.

Other University of Virginia trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT03207893.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing