Last updated: April 4, 2024
Sponsor: Oregon Health and Science University
Overall Status: Active - Recruiting
Phase
4
Condition
Dementia
Memory Loss
Mild Cognitive Impairment
Treatment
Sevoflurane
Propofol
Clinical Study ID
NCT06036095
STUDY00024667
Ages 70-110 All Genders Accepts Healthy Volunteers
Study Summary
Eligibility Criteria
Inclusion
Inclusion criteria:
- Men and women ≥ 70 years
- Sufficient vision and hearing to complete all tests
- Proficient in spoken and written English
- Scheduled for elective, inpatient, noncardiac surgery, expected to last at least 120minutes requiring general anesthesia
Exclusion
Exclusion criteria:
- Urgent or emergent surgery
- Diagnosed dementia (or MoCA<19)
- History of Parkinson's disease, major psychiatric disease (Schizophrenia), or severetraumatic brain injury
- Ongoing alcohol or substance abuse (per DSM V criteria)
- Allergy to propofol or sevoflurane
- Personal or family history of malignant hyperthermia
- Planned postoperative intubation
- Brain surgery
- Surgery requiring TIVA or GAS (i.e. cases involving neuromonitoring)
- Surgical procedure requiring general anesthetic occurring within 3 months (before orafter) surgical date
- Any patient or perioperative factor considered a contraindication to randomization toeither experimental group by the surgeon or anesthesiologist.
Study Design
Total Participants: 260
Treatment Group(s): 2
Primary Treatment: Sevoflurane
Phase: 4
Study Start date:
August 14, 2023
Estimated Completion Date:
March 15, 2027
Study Description
Connect with a study center
Oregon Health & Science University
Portland, Oregon 97239
United StatesActive - Recruiting

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