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NCT05781581 Clinical Trial

A Retrospective Cohort Study for Main Postoperative Complications After SARS-CoV-2 Infection

Liver Cancer Clinical Trial

Official title:
Main Postoperative Complications After SARS-CoV-2 Infection: A Retrospective Cohort Study

Clinical Trial Details — Status: Not yet recruiting

Administrative data
NCT number NCT05781581
Other study ID # retro-MPOC
Secondary ID
Status Not yet recruiting
Phase
First received
Last updated
Start date March 19, 2023
Est. completion date December 31, 2024

Study information
Verified date March 2023
Source RenJi Hospital
Contact Diansan Su, MD,PHD
Phone +8618616514088
Email diansansu@yahoo.com
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

To explore the relationship between SARS-CoV-2 infection in different time before operation and postoperative main complications (mortality, main pulmonary and cardiovascular complications) 30 days after operation; To determine the best timing of surgery after SARS-CoV-2 infection.

Recruitment information / eligibility
Status Not yet recruiting
Enrollment 50000
Est. completion date December 31, 2024
Est. primary completion date August 31, 2023
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Age=18 years; - Patients undergoing any type of surgery in operating room. Exclusion Criteria: - Surgery under local anesthesia (without participation of anesthetist) - Surgery outside the operating room, such as gastrointestinal endoscopy, puncture biopsy, etc - Patients who cannot determine whether they have had SARS CoV-2 infection before surgery.

Study Design

Related Conditions & MeSH terms

Intervention

Other:
• no intervention
no intervention

Locations
Country Name City State
n/a

Sponsors (5)
Lead Sponsor Collaborator
RenJi Hospital First Affiliated Hospital of Chongqing Medical University, Second Hospital of Shanxi Medical University, Sichuan Academy of Medical Sciences, The First Affiliated Hospital of Anhui Medical University

Outcome
Type Measure Description Time frame Safety issue
Primary All-cause mortality at 30 days after operation All-cause mortality at 30 days after operation 30 days after surgery
Secondary Main pulmonary complications at 30 days after operation a composite of postoperative pneumonia, acute respiratory distress syndrome (ARDS) and unexpected ventilation 30 days after surgery
Secondary Major Adverse Cardiovascular Events (MACE) a composite of cardiogenic death, myocardial infarction, new-onset heart failure or cardiogenic shock, and cerebrovascular accident (CVA) 30 days after surgery
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