COVID-19 (SARS-CoV-2 infection) detection in minimally invasive surgery Respiratory COVID-19 (SARS-CoV-2 infection), minimally invasive surgery
Conditions
Interventions
This is an observational trial. The study aims at analyzing with PCR the bioaerosol collected through the Biosampler (SKC Inc, AMS Analitica) in solution during 20 consecutive major laparoscopic surgi
Sponsors
Azienda Sanitaria Unità Locale di Reggio Emilia
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: 1. Diagnosis of COVID-19 confirmed through positive RT-PCR test before surgery 2. Scheduled laparoscopic procedure at least 1.5 h duration with major vessels exposure 3. Aged 18 to 90 years
Exclusion criteria
Exclusion criteria: Patients not able to give their informed consent
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Correct detection of the presence of SARS-CoV-2 virus particles collected in surgical smoke during laparoscopic surgery through highly efficient Biosamplers and RT-PCR test when compared to the presence of SARS-CoV-2 RNA detected in plasma using RT-PCR in the same cohort prior to the procedure | — |
Secondary
| Measure | Time frame |
|---|---|
| There are no secondary outcome measures | — |
Countries
Italy
Contacts
Public ContactRuggero Bollino
Outcome results
None listed