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NCT05671952 Clinical Trial

Multi-center Study on Reducing Postoperative Pulmonary Complications in Elderly Patients

Postoperative Pulmonary Complications Clinical Trial

Official title:
Multi-center Study on Reducing Postoperative Pulmonary Complications in Elderly Patients Based on Comprehensive Intervention System

Clinical Trial Details — Status: Not yet recruiting

Administrative data
NCT number NCT05671952
Other study ID # PPC20221203
Secondary ID
Status Not yet recruiting
Phase N/A
First received
Last updated
Start date January 2023
Est. completion date May 2023

Study information
Verified date December 2022
Source Wuhan Union Hospital, China
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this study is to carry out demonstrative comprehensive intervention for elderly patients in several hospitals to observe whether it can reduce the incidence and mortality of perioperative pulmonary complications in elderly patients and improve their perioperative prognosis.

Description:

This study investigated the incidence of postoperative pulmonary complications in various hospitals, and carried out demonstrative comprehensive intervention for elderly patients in several hospitals according to the comprehensive intervention system program of perioperative pulmonary complications, to observe whether the perioperative prognosis can be improved and the quality of life can be improved, thus verifying and optimizing the current evaluation system and intervention system, and providing evidence support for further extensive application.

Recruitment information / eligibility
Status Not yet recruiting
Enrollment 5000
Est. completion date May 2023
Est. primary completion date May 2023
Accepts healthy volunteers No
Gender All
Age group 65 Years and older
Eligibility Inclusion Criteria: 1. age 65 years or older 2. receiving invasive ventilation during general anesthesia for surgery Exclusion Criteria: 1. preoperative mechanical ventilation 2. procedures related to a previous surgical complication 3. a second operation after surgery 4. organ transplantation 5. discharged within 24 hours after surgery

Study Design

Related Conditions & MeSH terms

  • Postoperative Pulmonary Complications

Intervention

Other:
• Application of integrated intervention system programs
Application of integrated intervention system programs

Locations
Country Name City State
n/a

Sponsors (5)
Lead Sponsor Collaborator
Wuhan Union Hospital, China Qinghai People's Hospital, Shanxi Cardiovascular Hospital, Shiyan Taihe Hospital, Wuhan Central Hospital

Outcome
Type Measure Description Time frame Safety issue
Primary Postoperative pulmonary complications within one week after surgery
Secondary Postoperative pulmonary complications 30 days after surgery
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