Intravenous Acetaminophen for Postoperative Delirium in Older Patients Recovering From Major Noncardiac Surgery

Trial statusNot yet recruiting
Trial phasePhase 2, Phase 3
Trial typeInterventional
Biological sexAll
Age65+
SponsorRenJi Hospital

About this trial

Investigators propose this multi-center randomised controlled study to test the preventive effect of intravenouse acetaminophen in delirium over 5 postoperative days among older patients recovering from major non-cardiac surgery.

Eligibility criteria

Qualifiers

Age ≥ 65 years.

Scheduled for non-cardiac major surgery with general anesthesia that is expected to last more than 2h.

ASA Physical Status I-III.

Weight >50 kg.

Disqualifiers

Pre-existing neuropsychiatric diseases (Alzheimer's disease, Schizophrenia, Parkinson's Disease, Seizures, etc.).

Pre-existing cognitive impairment (MMSE<18).

Preoperative delirium.

Severe circulatory instability (preoperative left ventricular ejection fraction less than 30%, unstable angina, severe coronary artery disease, sick sinus syndrome, etc.).

Trial design

Treatments tested in this trial

  • Acetaminophen
  • Saline

Treatment groups

1,930 Participants
are divided into 2 treatment groups

Locations

This trial has no locations

Sponsors and collaborators