Actively Recruiting
Sex-Dependent Risk of Postoperative Delirium and Mediating Effects of Family Visits: A Prospective Observational Study
Led by Julian Rössler · Updated on 2026-06-01
471
Participants Needed
1
Research Sites
N/A
Total Duration
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AI-Summary
What this Trial Is About
Postoperative delirium is a frequent and serious problem affecting 10-40% of older adults undergoing non-cardiac surgery lasting at least 2 hours under general or spinal anesthesia. This observational study aims to explore whether women aged 65 years or older have a higher risk of developing postoperative delirium compared to men. Researchers will also investigate whether the amount of family visits differs between sexes and whether this might explain differences in delirium risk. The study will enroll 471 patients aged 65 and above scheduled for non-cardiac surgery. Delirium will be assessed twice daily from the first to the third postoperative day, or until discharge, using the 4 A's Test (4AT). Family visits will be recorded anonymously in the patient’s room during the same period. All participants will receive standard clinical care with no experimental treatments involved. Participants will be monitored closely with assessments of delirium and family visitation frequency during the hospital stay. Researchers will collect data on these measures to understand their relationship and impact on delirium risk. The study allows voluntary participation and withdrawal at any time without affecting medical care, and the total observation period for each participant covers up to three days post-surgery or until hospital discharge.
CONDITIONS
Brief Title
Sex-Dependent Risk of Postoperative Delirium and Mediating Effects of Family Visits
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Provided informed consent documented by signature
- Aged 65 years or older
- Scheduled for non-cardiac surgery expected to last 2 hours or more
- Surgery to be performed under general or spinal anesthesia
You will not qualify if you...
- Known drug or alcohol abuse
- Need for ventilation after surgery
- Currently participating in another study with an investigational drug
- Unable to complete study assessments
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - Day of surgery
Participants undergo scheduled non-cardiac surgery expected to last 2 hours or more under general or spinal anesthesia, followed by immediate post-operative care.
1 visit (in-person)
Duration - Up to 3 days or until discharge
Participants are monitored for postoperative delirium and family visits starting on postoperative day 1 and continuing until day 3 or discharge, whichever comes first.
Daily visits for up to 3 days
Trial Site Locations
Total: 1 location
1
Universitätsspital Zürich
Zurich, Switzerland
Actively Recruiting
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
2
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