Viewing Study NCT06307717



Ignite Creation Date: 2024-05-06 @ 8:14 PM
Last Modification Date: 2024-10-26 @ 3:23 PM
Study NCT ID: NCT06307717
Status: COMPLETED
Last Update Posted: 2024-04-10
First Post: 2024-03-06

Brief Title: Effects of Volatile Anaesthetics on Incidence of Postoperative Depression and Anxiety in Elderly Patients
Sponsor: Chinese PLA General Hospital
Organization: Chinese PLA General Hospital

Study Overview

Official Title: Volatile Anaesthetics on Incidence of Postoperative Depression and Anxiety
Status: COMPLETED
Status Verified Date: 2024-04
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: This study is a retrospective analysis of a large-scale multicentre prospective cohort study that investigates the impact of volatile anaesthetics on the incidence of postoperative depression and anxiety among elderly patients
Detailed Description: Studies have suggested volatile anaesthetics may alleviate depression and anxiety in patients However there is a paucity of research in this area The investigatorswanted to determine the association between volatile anaesthetics and depressionanxiety in elderly patients within 7 days after surgery

This study retrospectively analysed data from a prospective database of patients aged 65 and above who underwent non-cardiac non-neurosurgical elective surgery in 18 tertiary hospitals across 10 provinces in China Patients receiving volatile anaesthetics received at least one volatile anaesthetic sevoflurane isoflurane desflurane and those who received non-volatile anaesthetics did not receive any volatile anaesthetic Binary logistic regression analyses were conducted and propensity score-matching PSM and subgroup analyses were also applied

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: False
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None