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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04430062
Other study ID # Covid19nr1
Secondary ID
Status Completed
Phase
First received
Last updated
Start date May 1, 2020
Est. completion date May 30, 2020

Study information

Verified date June 2020
Source Azienda Socio Sanitaria Territoriale di Lodi
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The investigators retrospectively evaluated all the patients operated in a high-risk community hospital from the first Italian case of Covid-19 (February 21st) to the April 10th (in order to have at least a 30-days follow-up). The investigators selected those patients who had a preoperative or post-operative positive Real Time - Polymerase Chain Reaction (RT-PCR) for SARS-CoV-2 and the clinical outcome of the participants was evaluated in term of need of Intensive Care Unit (ICU) post-operative recovery, medical and surgical complications, length of hospital stay and death.


Recruitment information / eligibility

Status Completed
Enrollment 14
Est. completion date May 30, 2020
Est. primary completion date May 20, 2020
Accepts healthy volunteers No
Gender All
Age group N/A and older
Eligibility Inclusion Criteria:

- preoperative or post-operative positive Real Time - Polymerase Chain Reaction (RT-PCR) for SARS-CoV-2

- surgical procedure in elective or acute care surgery performed under general anesthesia

Exclusion Criteria:

- patients operated without general anesthesia

- patients preoperatively intubated for Covid-19

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Surgical procedures performed under general anesthesia
Surgical procedures performed under general anesthesia in patients with perioperative SARS-CoV-2 infection

Locations

Country Name City State
Italy Ospedale di Lodi - ASST Lodi Lodi Lombardia

Sponsors (1)

Lead Sponsor Collaborator
Azienda Socio Sanitaria Territoriale di Lodi

Country where clinical trial is conducted

Italy, 

Outcome

Type Measure Description Time frame Safety issue
Primary Mortality 30 days
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