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Building a Platform for Precision Anesthesia in the Geriatric Surgical Patient

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Stanford University

Status

Enrolling

Conditions

Anesthesia; Adverse Effect
Cognitive Change
Cognitive Impairment
Anesthesia; Reaction
Cognitive Decline
Postoperative Delirium

Treatments

Combination Product: Neurocognition Interventions

Study type

Observational

Funder types

Other

Identifiers

Details and patient eligibility

About

The research team is creating a foundational infrastructure in order to develop a precision medicine approach for geriatric patients who require surgery with anesthesia. The team plans to build the first of its kind comprehensive database of demographic and risk factor questionnaire responses, biobanked blood specimens, intraoperative electroencephalography (EEG), and inclusive cognitive testing throughout patient interaction starting at the preop appointment until a year later. This will be used to create a predictive model of periooperative neurocognitive disorders.

Enrollment

250 estimated patients

Sex

All

Ages

65+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • At least 65 years old (inclusive)
  • Non cardiac general elective surgery
  • General anesthesia is expected for 2+ hours

Exclusion criteria

  • Alzheimer's
  • Dementia
  • Parkinson's
  • History of neurodegenerative diseases
  • Medication for depression (ie. Benzodiazepines)
  • Alcoholism
  • Discretion of PI

Trial design

250 participants in 1 patient group

Neurocognitive Assessment Arm
Treatment:
Combination Product: Neurocognition Interventions

Trial contacts and locations

1

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Central trial contact

Samantha M Gaston, BS

Data sourced from clinicaltrials.gov

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