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Continuous Glucose Monitoring (CGM) in an Underserved Population

Recruiting

Continuous Glucose Monitoring in an Underserved Population: Impact on Glucose Control, Patient Reported Outcomes, Healthcare Utilization, and Long Term Complications

Who can join

Ages 18 to 75 · All sexes

Full eligibility criteria
Inclusion Criteria:

* Age 18-75 years
* Type 2 diabetes mellitus
* HbA1C ≥ 7.5%
* At least on 1 insulin injection therapy daily
* Patients established with primary care clinic or endocrinology clinic or diabetes clinics in the New Orleans and surrounding areas
* Patients with Medicaid or free care or uninsured
* Patients must be able to speak and understand English and be capable of providing informed consent to participate in the study

Exclusion Criteria:

* Type 1 diabetes mellitus
* Currently on CGM or using insulin pump
* Advanced renal disease or Estimated Glomerular Filtration Rate (eGFR) \<40
* Serious co-morbidities which in the investigator's opinion, will make it challenging for patients to participate
* The patient has been diagnosed with end-stage renal disease, is on dialysis, or has had a kidney transplant, Hemoglobinopathies, iron therapy or other condition that interferes with HbA1c measurement
* Pregnant

About the study

The investigators aim is to conduct a randomized clinical trial in an underserved population who are either uninsured or on Medicaid and taking at least one injection of insulin daily. The investigators believe that this study will lead to considerable alleviation of health disparities and provide better care for an underserved population. This will be a pilot study to evaluate the feasibility of such a trial in this population before doing a larger multicenter trial.

What is being tested

Sponsor: Tulane University · Participants: 50 · Started: Mar 19, 2026

Contact the study team

Official record on ClinicalTrials.gov — NCT07135531

Locations in the U.S.

LouisianaUniversity Medical Center, New Orleans

Conditions

From ClinicalTrials.gov, data retrieved Sep 30, 2026. Each study sets its own eligibility; the study team decides who can join.