A Study Of Glucagon-Like Peptide-1 Receptor Agonists In Postoperative Delirium

Overview

About this study

The purpose of this study is to evaluate the impact that GLP-1 RAs have on the incidence and phenotype of postoperative delirium.

Participation eligibility

Participant eligibility includes age, gender, type and stage of disease, and previous treatments or health concerns. Guidelines differ from study to study, and identify who can or cannot participate. There is no guarantee that every individual who qualifies and wants to participate in a trial will be enrolled. Contact the study team to discuss study eligibility and potential participation.

Inclusion Criteria:

  • 60 years of age or older with diagnosis of T2DM

  • Planned to undergo non-cardiac, non-intracranial surgery

  • Estimated length of stay > 24 hours in the hospital

Exclusion Criteria :

  • Patient declines participation in the study

  • Patient lacks capacity to consent

  • Unable to communicate or participate in delirium assessments due to language barriers or sensory deficits (delirium assessments are not validated in languages other than English or with use of interpreter)

  • Incarcerated

  • Baseline encephalopathy or prior diagnosis of major neurocognitive disorder, including moderate or severe dementia

  • History of delirium

  • Acute neurologic injury within the preceding 6 months

Note: Other protocol defined Inclusion/Exclusion Criteria may apply.

Eligibility last updated 05/11/2026. Questions regarding updates should be directed to the study team contact.

Participating Mayo Clinic locations

Study statuses change often. Please contact the study team for the most up-to-date information regarding possible participation.

Mayo Clinic Location Status

Rochester, Minn.

Mayo Clinic principal investigator

Lindsay Guevara, M.D.

Contact us for the latest status

More information

Publications

Publications are currently not available

Additional contact information

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Phone: 800-664-4542 (toll-free)

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