RecruitingNot ApplicableNCT07063420

Patient Centered Multi-Agent Decision Support System (PCM-DSS) for Healthcare Providers

Patient Centered Multi-Agent Decision Support System (PCM-DSS) for Healthcare Providers: A Pilot Study

Sponsor

Daniel Chernavvsky, MD

Enrollment

18 participants

Start Date

Oct 28, 2025

Study Type

INTERVENTIONAL

Conditions

Decision Support System (Software) for multi antidiabetic drug therapy use in type 2 diabetes (T2D).

Min Age: 18 Years

Age ≥18.0 years old at time of consent.
Clinical diagnosis, based on investigator assessment, of type 2 diabetes for at least 6 months.
Hemoglobin A1c (HbA1c) ≥ 7.0%.
Currently using an approved long-acting insulin for at least 3 months (e.g., insulin glargine, insulin degludec).
Treated or about to be treated with multi-drug therapies for T2D.
If using a CGM, willingness to wear an additional study CGM during the duration of the study.
Access to the internet and willingness to upload data during the study as needed.
If female and sexually active, must agree to use a form of contraception to prevent pregnancy while a participant in the study. A negative serum or urine pregnancy test will be required for all females who self-report that they are of childbearing potential. Participants who become pregnant will be discontinued from the study. Also, participants who during the study develop and express the intention to become pregnant within the timespan of the study will be discontinued.

Currently using rapid insulin for at least three months (e.g., insulin aspart, insulin lispro, insulin regular).
Currently being treated for a seizure disorder.
A known medical condition that in the judgment of the investigator might interfere with the completion of the protocol, such as but not limited to, the following examples:
Seizure disease
Decompensated cardiac disease
Inpatient psychiatric treatment in the past 6 months
Presence of a known adrenal disorder
Currently pregnant or intent to become pregnant during the trial.
Anticipated surgical, interventional procedures or prolonged periods of fasting during this study.