Actively Recruiting

Age: 65Years +
All Genders
ID07502391

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

On this page

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

Age: 65Years +
All Genders

Eligibility Criteria

Eligible

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
Not Eligible

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

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Surgery and Immediate Post-operative Care

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)

Post-operative Follow-up

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

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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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