Official Title
A Cohort Study to Assess the Effectiveness of Preoperative Shielding and N/T RT-PCR Swabbing for Elective Cancer Surgery Patients in the COVID-19 Pandemic
Brief Summary

trial to assess the effectiveness of pre-operative screening for COVID-19 in patients undergoing elective cancer surgery.

Detailed Description

1. Background:

The optimal method of screening patients for COVID infection before elective cancer
surgery is unclear. Provisional data from the international COVIDsurg audit as well as a
similar study from China has shown mortality rates of in excess of 20% for COVID +ve
patients undergoing surgery and so ensuring patients do not have infection before
surgery is critical (1).

Current practice for the preoperative screening of elective surgical patients involves a
period of self-isolation, assessment of self-reported symptoms and nose and throat swab
testing. Many patients are asymptomatic with COVID and the false negative rate of RT-PCR
nose and throat swabs may be as high as 30% (2,3). Furthermore, we do not know how
effective our strategy is at preventing hospital acquired COVID in the days after
surgery. Patients are currently going to designated clean (silver) wards postoperatively
to reduce this risk with other patient who have tested negatively to the above screening
process too

2. Rationale:

The aim of this study is to assess the rate of perioperative COVID in elective surgical
patients, and to assess whether RT-PCR swabbing adds any additional value i.e. does it detect
clinically important asymptomatic patients.

If asymptomatic patients are diagnosed preoperatively this will reduce perioperative
morbidity and mortality as well as confirming this as an appropriate preoperative screening
process. Alternatively, should nose and throat swabbing not improve the diagnosis of COVID-19
in asymptomatic patients this trial may stop unnecessary visit to the hospital where they may
be more likely to contract COVID-19 and reduce the use of a limited resource.

Unknown status
COVID19
Cancer

Other: pre-operative screening

reported symptoms plus nose and throat swabbing 48 hrs prior to surgery

Other: telephone consult

telephone consult 14 days (+/- 2 days) to assess for any COVID-19 symptoms

Eligibility Criteria

Inclusion Criteria:

- participants capable of giving informed consent,

- gender: Male and Female

- Age: 18 years and above

- Preoperative cancer patients (elective)

- Willing to be contacted by phone after hospital discharge

- Patients listed for inpatient admission postoperatively (cancer patients)

Exclusion Criteria:

- Cancer patients who require non-cancer surgery

- emergency cancer operations

- Patients under the age of 18

- Patients who do not have capacity to consent

- Cancer patients not requiring an inpatient stay postoperatively

- Patients who it was not anticipated would require an inpatient stay preoperatively but
required admission after surgery

Eligibility Gender
All
Eligibility Age
Minimum: 18 Years ~ Maximum: N/A
Countries
United Kingdom
Locations

Liverpool University Hospitals NHS Foundation Trust
Liverpool, Merseyside, United Kingdom

Investigator: Robert Jones, MBChB
Contact: 0151 525 5980
robert.jones@liverpool.ac.uk

Investigator:

Contacts

Robert Jones, MBChB
0151 525 5980
robert.jones@liverpool.ac.uk

Peter Gaskell, MBChB
0151 525 5980
p.gaskell@doctors.org.uk

Robert Jones, MBChB, Principal Investigator
Liverpool University Hospitals NHS Foundation Trust

Liverpool University Hospitals NHS Foundation Trust
NCT Number
MeSH Terms
COVID-19