Mitigating Delirium With Fluvoxamine Treatment for Non-Cardiac Surgery
RecruitingPhase 3
Mitigating Delirium With Fluvoxamine Treatment for Non-Cardiac Surgery (MD FluNCS)
Who can join
Ages 60 and older · All sexes
Full eligibility criteria
Inclusion Criteria: * English-speaking * elective non-cardiac or non-intracranial surgery requiring at least a 2-day hospital length of stay Exclusion Criteria: * Received investigational drug within the last 7 weeks * lack of capacity to provide informed consent * prior known intolerance or allergy to SSRIs or fluvoxamine * planned postoperative ventilation * drug or alcohol dependence * preoperative use of non-NSAID medications with drug-drug interactions of Class X (Avoid Combination) or D (Consider Therapy Modification) * risk of serotonin syndrome (St John's Wort, SSRIs, or TCA)
About the study
The investigation will establish biological plausibility and infrastructure required for a multisite clinical trial evaluating the re-purposing of fluvoxamine to mitigate postoperative delirium risk in geriatric patients undergoing non-cardiac non-intracranial surgery.
What is being tested
- Fluvoxamine (drug)
- Placebo (drug)
Sponsor: Washington University School of Medicine · Participants: 46 · Started: Apr 6, 2026
Contact the study team
- Sarah Knarr · Phone: 3143622415
Official record on ClinicalTrials.gov — NCT06969287
Locations in the U.S.
| Missouri | Washington University School of Medicine/Barnes-Jewish Hospital, St Louis |
Conditions
From ClinicalTrials.gov, data retrieved Sep 30, 2026. Each study sets its own eligibility; the study team decides who can join.