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

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

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05682898
Enrollment
300
Registered
2023-01-12
Start date
2023-01-15
Completion date
2024-06-01
Last updated
2023-01-12

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Colorectal Cancer, Surgical Procedure, Unspecified

Brief summary

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.

Interventions

PROCEDURETiming of colorectal cancer surgery

The timing of colorectal cancer surgery is different according patients' different conditions which is difined as more than 7 weeks or less than 7 weeks.

Sponsors

Changhai Hospital
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Healthy volunteers
Yes

Inclusion criteria

* undergoing colorectal cancer surgery * infected with COVID-19 but nucleic acid test result is negative * the patients compliance is good * signed the consents voluntarily

Exclusion criteria

* undergoing emergency surgery(intestinal obstruction, intestinal perforation, intestinal hemorrhage, et al.) * The patients' situations which judged by situations is not suitable to participate in the clinical trial

Design outcomes

Primary

MeasureTime frameDescription
Incidence of surgical complications30 days after surgeryComplications including: intraperitoneal hemorrhage, anastomotic leak, anastomotic bleeding, abdominal infection, pulmonary infection, chylous fistula, intestinal obstruction, et al.

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026