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NCT04389008 Clinical Trial

The Study of Anesthesia-related Risk Factors for Postoperative Death in Elderly Non-cardiac Surgery Patients in China

Anesthesia Clinical Trial

Official title:
The Study of Anesthesia-related Risk Factors for Postoperative Death in Elderly Non-cardiac Surgery Patients in China: a Multi-center Retrospective Study Based on Database

Clinical Trial Details — Status: Enrolling by invitation

Administrative data
NCT number NCT04389008
Other study ID # PLAGHAOC202001
Secondary ID
Status Enrolling by invitation
Phase
First received
Last updated
Start date May 31, 2020
Est. completion date December 31, 2021

Study information
Verified date June 2021
Source Chinese PLA General Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

At present, the elderly population in China has reached 241 million, and there are more than 20 million elderly surgical patients every year, accounting for about 25% of the surgical population. However, there is no research report on the anesthesia related risk factors of death of elderly patients in hospital. The purpose of this study is to analyze the perioperative data of multicenter database, and to explore the anesthesia related death risk factors of elderly patients with noncardiac surgery in the investigator's country, especially within 24 hours after surgery, so as to help improve the anesthesia management technology of elderly patients during surgery, improve the medical quality of perioperative period, and improve the prognosis of patients.

Recruitment information / eligibility
Status Enrolling by invitation
Enrollment 300000
Est. completion date December 31, 2021
Est. primary completion date September 1, 2021
Accepts healthy volunteers No
Gender All
Age group 65 Years and older
Eligibility Inclusion Criteria: - 1.patients larger than 65 years old at the time of surgery 2.Patients hospitalized for surgery between Jua 2008 to April 2020 Exclusion Criteria: - 1.Critical demographic information and course records are inaccurate or missing. 2.The outcome could not be determined during the hospitalization. 3.Cardiac surgery patients 4.Patients undergoing surgery under local anesthesia

Study Design

Related Conditions & MeSH terms

Intervention

Other:
• no interventions
no interventions

Locations
Country Name City State
China Chinese PLA General Hospital Beijing Haidian

Sponsors (1)
Lead Sponsor Collaborator
Chinese PLA General Hospital

Country where clinical trial is conducted

China, 

Outcome
Type Measure Description Time frame Safety issue
Primary Whether death occurred during hospitalization after surgery Whether death occurred during hospitalization after surgery Within 30 days after discharge
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