What this study is
Simplified from ClinicalTrials.govTesting a continuous glucose (blood sugar) monitor started before hospital discharge to improve blood sugar control at home, in hospitalized adults with type 2 diabetes and an HbA1c of 9% or higher who take insulin and/or oral diabetes medicines, expect to go home, and don't already use one. It is compared with finger-stick checks.
Read the original summary from ClinicalTrials.gov
The TRANSITION-CGM trial will evaluate whether starting continuous glucose monitoring (CGM) before hospital discharge improves blood glucose control in adults with type 2 diabetes compared with usual care using finger-stick blood glucose checks. The study focuses on the transition from hospital to home, when patients may face changes in diabetes medications and challenges managing their blood glucose levels.
This single-center, randomized controlled trial will enroll approximately 218 adults with type 2 diabetes, a hemoglobin A1c (HbA1c) 9% and above, and treatment with insulin and/or oral diabetes medications. Participants will be recruited during hospitalization and must be expected to return home after discharge. People already using a CGM will not be eligible.
Participants will be randomly assigned in equal numbers to one of two groups. The CGM group will start using a continuous glucose monitor before discharge and receive device training and written instructions. The usual-care group will continue finger-stick blood glucose monitoring and receive standard discharge education. Both groups will receive assistance with outpatient diabetes follow-up. Diabetes medications will be managed by treating clinicians according to usual clinical practice.
Participants will be followed for approximately 12 weeks after discharge, with an early follow-up encounter and a final assessment at 12 weeks. The primary outcome is HbA1c at 12 weeks, a blood test that reflects average blood glucose levels over approximately three months. Secondary outcomes include diabetes-related hospitalizations and episodes of low blood sugar. Additional exploratory measures include CGM use, follow-up attendance, patient-reported experiences, and time spent within the target glucose range when CGM data are available.
The study will determine whether initiating CGM during hospitalization can improve glycemic control after discharge and provide preliminary evidence about its effects on diabetes-related hospitalizations and hypoglycemia.
What's being tested
- Continuous glucose monitor
Intervention · DEVICE
Participants in the intervention arm will be educated and discharged from their hospitalization with a continuous glucose monitor and followed up in clinic.
Study details
- Sponsor
- University of Cincinnati
- Conditions
- Type 2 Diabetes
- Enrolling
- 218 people
- Starts
- 2026-11
- Est. completion
- 2028-03
- Design
- Open-label, randomized, parallel groups
- Record
- View on ClinicalTrials.gov ↗
Who can join
Age 18 Years and overSex ALLHealthy volunteers Not acceptedYou may qualify if
- Age ≥ 18 years
- Established or new diagnosis of type 2 diabetes mellitus (T2DM)
- HbA1C >/= 9%
- On insulin therapy and/or oral hypoglycemic agents at time of index hospitalization
- Anticipated discharge to home within 48-72 hours
- Ability to provide informed consent and attend 12-week follow-up
You can't join if
- Active psychiatric illness that interferes with consent or study adherence
- Cognitive disturbance/dementia impairing device use or self-care
- Housing instability
- Skilled nursing facility (SNF) admission or planned discharge to SNF
- Contraindication to CGM placement (e.g., severe skin allergy)
- Pre-existing established CGM use
- Pregnancy
- ESRD
- Steroid use (Prednisone equivalent 10 mg/day or more)
- HgbA1C < 9%
- Hemoglobinopathy (where HgbA1C is not reliable)
Sign in and we'll check these against your records.Full criteria on ClinicalTrials.gov ↗
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Study locations (1)
1 openUniversity of Cincinnati Medical Center
Cincinnati, Ohio, United States
- Arunab H Mehta, MD, MEd · Contact3129343095mehtaab@ucmail.uc.edu
- Lexi Harrison, BS · Contactharrislx@mail.uc.edu
- Arunab H Mehta, MD, MED · Principal investigator
- Houman Varghai, MD · Principal investigator
- Mercedes Falciglia, MD · Sub-investigator
Study team
Sponsor
University of Cincinnati
Study ID 2026-0491
Study director
Mercedes Falciglia, MD
University of Cincinnati
Principal investigator
Arunab H Mehta, MD, MEd
University of Cincinnati
Principal investigator
Houman Varghai, MD
University of Cincinnati
Frequently asked questions
The sponsor hasn't published answers to common questions for this trial.