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Impact of Perioperative Hyperoxia on Cancer Recurrence and Mortality After Elective Colorectal Cancer Surgery

Impact of Perioperative Hyperoxia on Cancer Recurrence and Mortality After Elective Colorectal Cancer Surgery

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06989346
Acronym
OncO2
Enrollment
403
Registered
2025-05-25
Start date
2024-05-17
Completion date
2025-04-11
Last updated
2025-05-25

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

Conditions

Colorectal Surgery, Hyperoxia, Mortality, Recurrence, Survival Rate

Keywords

Hyperoxia, Recurrence-free Survival, Colorectal Surgery

Brief summary

The goal of this observational study is to evaluate whether perioperative hyperoxia (FiO₂ \> 0.8), compared to conventional oxygen therapy (FiO₂ \< 0.4), is associated with increased cancer recurrence and mortality in patients undergoing curative elective colorectal cancer surgery.

Detailed description

In 2016, the World Health Organization (WHO) recommended the use of perioperative hyperoxia (FiO₂ \> 0.8) to reduce the risk of postoperative surgical site infections (SSIs). However, the WHO also highlighted potential adverse effects associated with hyperoxia, including increased cancer recurrence and mortality. This study aims to evaluate whether perioperative hyperoxia (FiO₂ \> 0.8), compared to conventional oxygen therapy (FiO₂ \< 0.4), is associated with increased cancer recurrence and mortality in patients undergoing curative elective colorectal cancer surgery. This study is a follow-up of a previously published cohort originally designed to assess whether FiO₂ \> 0.8 was associated with a higher incidence of perioperative cardiovascular complications. In this follow-up, oncological recurrence and mortality events were recorded at least three years after the index surgery. The primary outcome was recurrence-free survival over the follow-up period, analyzed using Kaplan-Meier curves and a Cox proportional hazards model. The secondary outcome was the 3-year mortality rate, analyzed using the Chi-square test.

Interventions

None listed

Sponsors

Parc de Salut Mar
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Patients over 18 years old; * Scheduled for major elective colorectal surgery under general anaesthesia with tracheal intubation.

Exclusion criteria

* Non-oncologic surgery or non-curative oncological surgery * Pregnant or breastfeeding women * Chronic obstructive pulmonary disease (forced expiratory volume in one second \<50% or in need of domiciliary oxygen thera-py) * Acute coronary event or stroke during the previous six weeks (before the surgery) * Chronic renal failure requiring renal replacement therapy; * Predicted length of stay of less than one day; * Any patient that has received general anaesthesia during the previous month.

Design outcomes

Primary

MeasureTime frameDescription
Recurrence-free SurvivalFollow-up period (at least 3 years since surgery)Length of time from the end of primary treatment (surgery in this case) until the evidence of cancer recurrence (locoregional or systemic) or death in the last follow-up

Secondary

MeasureTime frameDescription
Mortality3-year follow-up periodPercentage of global mortality (not exclusively related to the oncologic disease)

Countries

Spain

Outcome results

None listed

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