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Glycemic Optimization On Discharge From the Emergency Room

NCT05197829 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 30

Last updated 2024-04-16

Study results available
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Summary

Continuous glucose monitors can help people with diabetes avoid blood sugar levels that are either dangerously high or low. This study evaluates whether continuous glucose monitoring after discharge from the emergency room can help people with type 1 or type 2 diabetes avoid repeat emergency room visits, achieve improved blood sugar control, and feel less distressed about managing their diabetes.

Conditions

Interventions

DEVICE

Continuous Glucose Monitoring

Participants in the experimental arm will receive an unblinded flash continuous glucose monitor.

OTHER

Care Coordination

All participants will receive diabetes education, written handouts, and help setting up ambulatory appointments.

Sponsors & Collaborators

  • Mark O'Connor

    lead OTHER

Principal Investigators

  • Mark J O'Connor, MD · University of Massachusetts, Worcester

Study Design

Allocation
RANDOMIZED
Purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2022-01-05
Primary Completion
2023-01-05
Completion
2024-01-05
FDA Device
Yes

Countries

  • United States

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05197829 on ClinicalTrials.gov