NCT06905366

Brief Summary

This study aims to assess the association between perioperative cognitive function and postoperative quality of recovery.

Trial Health

35
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
140

participants targeted

Target at P50-P75 for all trials

Timeline
Completed

Started May 2025

Shorter than P25 for all trials

Status
not yet recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

March 25, 2025

Completed
7 days until next milestone

First Posted

Study publicly available on registry

April 1, 2025

Completed
1 month until next milestone

Study Start

First participant enrolled

May 1, 2025

Completed
7 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 1, 2025

Completed
2 months until next milestone

Study Completion

Last participant's last visit for all outcomes

February 1, 2026

Completed
Last Updated

April 1, 2025

Status Verified

March 1, 2025

Enrollment Period

7 months

First QC Date

March 25, 2025

Last Update Submit

March 25, 2025

Conditions

Perioperative Neurocognitive DisordersPostoperative Quality of Recovery

Keywords

cognitive function

Outcome Measures

Primary Outcomes (1)

  • QoR-15GE

    postoperative quality of recovery

    first postoperative day

Study Arms (1)

cognition

patients, who will undergo preoperative and postoperative assessment for cognitive function

Eligibility Criteria

Age65 Years+
Sexall
Healthy VolunteersNo
Age GroupsOlder Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

patients aged 65 years or older, who are scheduled for elective non-cardiac surgery

You may qualify if:

  • elective non-cardiac surgery
  • age ≥65 years
  • duration of surgery ≥60 years

You may not qualify if:

  • inability to give informed consent

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

March 25, 2025

First Posted

April 1, 2025

Study Start

May 1, 2025

Primary Completion

December 1, 2025

Study Completion

February 1, 2026

Last Updated

April 1, 2025

Record last verified: 2025-03

Data Sharing

IPD Sharing
Will not share