Clinical Trials Directory

Trials / Recruiting

RecruitingNCT06182215

PostoperAtive Neurocognitive Dysfunction After Major AbdomiNal Surgery (PANDAMAN)

Postoperative Neurocognitive Dysfunction After Major Abdominal Surgery: A Prospective Observational Cohort Study

Status
Recruiting
Phase
Study type
Observational
Enrollment
500 (estimated)
Sponsor
Sixth Affiliated Hospital, Sun Yat-sen University · Academic / Other
Sex
All
Age
65 Years – 90 Years
Healthy volunteers
Not accepted

Summary

Predisposing and precipitating factors for perioperative delirium for the elderly remain elusive. This research will be conducted to determine risk factors of postoperative delirium.

Detailed description

This study intends to include 500 participants over 65 years old undergoing elective abdominal major surgery. The primary outcome is incidence of delirium at 7 days postoperatively, and the secondary outcomes include preoperative sleep disorders(Athens In-somnia Scale, AIS), postoperative cognitive impairment (Abbreviated Mental Test Score, AMTS), postoperative pain (NRS pain score), incidence of significant postoperative complications, length of hospital stay, and serum biomarkers levels.

Conditions

Timeline

Start date
2023-12-11
Primary completion
2025-12-31
Completion
2026-12-31
First posted
2023-12-26
Last updated
2024-06-17

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT06182215. Inclusion in this directory is not an endorsement.