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NCT05682898

Perioperative Management of Colorectal Cancer Patients Infected With COVID-19: a Multicenter Prospective Cohort Study.

Status unknown Last updated 12 January 2023
What this trial tests

trial testing Timing of colorectal cancer surgery in Colorectal Cancer in 300 participants. Status unknown.

Timeline
15 January 2023
Primary endpoint
1 January 2024
1 June 2024

Quick facts

Lead sponsorChanghai Hospital
StatusStatus unknown
Study typeOBSERVATIONAL
Enrollment300
Start date15 January 2023
Primary completion1 January 2024
Estimated completion1 June 2024

Drugs / interventions tested

Conditions studied

Sponsor

Changhai Hospital

Who can join

Eligibility, any sex, with Colorectal Cancer or Surgical Procedure, Unspecified. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This trial is a multicenter prospective cohort study to explore timing of colorectal cancer surgery after COVID-19 infection so that can assist clinicians and patients. Currently, there is less evidence on perioperative outcomes after COVID-19 vaccination and the omicron variant. Therefore, it is necessary to update previously published consensus which recommends that patients should avoid elective surgery within 7 weeks of COVID-19 infection remain, unless the benefits of doing so exceed the risk of waiting. Aiming at the above problems, we plan to carry out a multicenter prospective cohort study to develop perioperative management according patients' different conditions.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Colorectal Cancer

Currently open trials in the same condition.

Other Changhai Hospital trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT05682898.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing