Promoting safer diabetes treatments for older adults

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This study aims to improve patient safety for older adults with type 2 diabetes who are currently prescribed sulfonylureas, a class of medications associated with adverse effects. The researchers will identify patients aged 45 and older taking sulfonylureas and empower them to discuss alternative treatments with their primary care providers. Additionally, primary care providers will receive education on contemporary diabetes treatment guidelines and the risks and benefits of various medication classes. The goal is to facilitate informed discussions and promote safer treatment options in ambulatory settings.

Why it matters

Who can join: the full rules

Inclusion Criteria:

* Age ≥ 45 years
* Type 2 diabetes (diagnosed on or before 12/31/2021)
* Current/active prescription for one or more SU medications
* Established care (≥2 visits) with UH primary care provider (PCP) since 2021

Exclusion Criteria:

* Type 1 diabetes
* PCP provides a reason why patient participation is inappropriate (e.g., known cost barriers without any alternatives, prior discussion with patient about alternatives, etc.)
* Patient unable or unwilling to have conversation with their PCP regarding SU
* Unable to provide informed consent

Where it's running

• University Hospitals Cleveland Medical Center
  Cleveland, Ohio, United States Recruiting

Study contacts

• Principal investigator: Ian Neeland, MD — University Hospital Cleveland Medical Center
• Study coordinator: Ian Neeland, MD
• Email: ian.neeland@uhhospitals.org
• Phone: 216-844-5965

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.