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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register.
Register: ChiCTR
Last refreshed on: 18 September 2023
Main ID:  ChiCTR2300075642
Date of registration: 2023-09-11
Prospective Registration: No
Primary sponsor: Yijishan Hospital, Wannan Medical College
Public title: Postoperative recovery quality in patients with SARS-CoV-2 (Omicron variant) infection at different surgical timing: a clinical study
Scientific title: Postoperative recovery quality in patients with SARS-CoV-2 (Omicron variant) infection: a clinical study
Date of first enrolment: 2023-05-30
Target sample size: The time of SARS-CoV-2 diagnosis was 0 to 2 weeks (including 2 weeks)from elective general anesthesia surgery:68;The time of SARS-CoV-2 diagnosis was 2 to 4 weeks (including 4 weeks)from elective general anesthesia surgery:99;The time of SARS-CoV-2 diagn
Recruitment status: Completed
URL:  https://www.chictr.org.cn/showproj.html?proj=199021
Study type:  Observational study
Study design:  Cohort study  
Phase:  N/A
Countries of recruitment
China
Contacts
Name: Chen Yongquan    
Address:  2 Zhe Shan West Road, Wuhu City, Anhui Province
Telephone: +86 139 5619 6920
Email: chenyq263@163.com
Affiliation:  Yijishan Hospital, Wannan Medical College
Name: Wang Qiubo    
Address:  2 Zhe Shan West Road, Wuhu City, Anhui Province
Telephone: +86 183 5535 2785
Email: 576430305@qq.com
Affiliation:  Yijishan Hospital, Wannan Medical College
Key inclusion & exclusion criteria
Inclusion criteria: ?age?18 years old,?ASA grades I~?,?For asymptomatic or mild patients diagnosed with SARS-CoV-2 infection 8 weeks before surgery, diagnosis: nasal swab or throat swab accounting antigen detection, as defined according to COVID-19 Prevention and Control Plan (eighth 8). If SARS-CoV-2 patients have multiple operations, the surgery closest to the time of diagnosis of SARS-CoV-2 infection was taken as the observation object,?can voluntarily cooperate with this study.
Exclusion criteria: ?People with mental illness,?Severe heart, lung, liver, and kidney dysfunction,? Hearing or communication impairment,?have participated in other researchers

Age minimum: 18
Age maximum: 85
Gender: Both
Health Condition(s) or Problem(s) studied
patients with SARS-CoV-2 infection
Intervention(s)
The time of SARS-CoV-2 diagnosis was 0 to 2 weeks (including 2 weeks)from elective general anesthesia surgery:N/A;The time of SARS-CoV-2 diagnosis was 2 to 4 weeks (including 4 weeks)from elective general anesthesia surgery:N/A;The time of SARS-CoV-2 diagnosis was 4 to 6 weeks (including 6 weeks)from elective general anesthesia surgery:N/A;The time of SARS-CoV-2 diagnosis was 6 to 8 weeks (including 8 weeks)from elective general anesthesia surgery:N/A;
Primary Outcome(s)
QoR-15;
Secondary Outcome(s)
Oxygenation index;Length of hospital stay;Postoperative complications;
Secondary ID(s)
Source(s) of Monetary Support
Graduate project
Secondary Sponsor(s)
Ethics review
Status: Approved
Approval date: 29/05/2023
Contact:
Wu Pei
+86 553 573 9209
Results
Results available:
Date Posted:
Date Completed:
URL:
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