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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT05701449
Other study ID # PPCS192023
Secondary ID
Status Not yet recruiting
Phase
First received
Last updated
Start date January 2023
Est. completion date December 2023

Study information

Verified date January 2023
Source Wuhan Union Hospital, China
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

This study aims to verify the prediction model of postoperative pulmonary complications by collecting clinical information on elderly patients. In addition, the incidence of postoperative pulmonary complications in elderly patients before and after using the prediction model was compared.


Description:

More than 300 million major operations are performed worldwide each year, and older patients account for about a third of elective operations. Compared with young people, the elderly are more prone to postoperative complications due to age-related degeneration of the physiological functions of various organs and tissues. Postoperative pulmonary complications, including pneumonia, atelectasis, and respiratory failure, are common. Even mild pulmonary complications can lead to the prolonged hospital stay and increased postoperative mortality. Although there have been many studies on postoperative lung complications, there have been few studies on elderly patients. In our country, the real incidence data of elderly patients after a perioperative period of pulmonary complications, the lack of effective prevention, intervention measures, and targeted prevention and treatment technology, these reasons lead to the clinical diagnosis and treatment of elderly patients after a perioperative period of pulmonary complications are very difficult. Therefore, the research team intends to verify the established prediction model of postoperative pulmonary complications and compare the incidence of postoperative pulmonary complications in elderly patients before and after using the prediction model.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 5000
Est. completion date December 2023
Est. primary completion date December 2023
Accepts healthy volunteers
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 within one week 4. organ transplantation 5. discharged within 24 hours after surgery

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
n/a

Sponsors (20)

Lead Sponsor Collaborator
Wuhan Union Hospital, China China-Japan Friendship Hospital, Chinese PLA General Hospital, Danjiangkou First Hospital, Dongfeng General Hospital of Chinese Medicine, First Affiliated Hospital of Guangxi Medical University, First Affiliated Hospital of Zhejiang University, Qinghai People's Hospital, Shanxi Cardiovascular Hospital, Shiyan City Renmin Hospital, Shiyan Integrated Traditional and Western Medicine Hospital, Shiyan Taihe Hospital, Shiyan Traditional Chinese Medicine Hospital, Suizhou Central Hospital, Wuhan No.1 Hospital, Xiangyang Central Hospital, Xiangyang No.1 People's Hospital, Yunxi Renmin Hospital, Yunyang Renmin Hospital, Zhuxi Renmin Hospital

Outcome

Type Measure Description Time frame Safety issue
Primary Postoperative pulmonary complications within one week after surgery
Secondary Length of postoperative hospital stay 6 weeks after surgery
Secondary Postoperative Death 6 weeks after surgery
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