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Oxygen Partial Pressure After Breast Cancer Surgery

Oxygen Partial Pressure After Breast Cancer Surgery

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05737446
Enrollment
60
Registered
2023-02-21
Start date
2023-02-23
Completion date
2024-06-01
Last updated
2023-03-29

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

Conditions

Breast Cancer, Hypoxia, Surgery-Complications

Keywords

Breast cancer surgery, postoperative hypoxia, Lung function

Brief summary

Hypoxia and reduced oxygen partial pressure is commonly occurring after abdominal surgery. This study aims to investigate whether similar changes also occur after breast cancer surgery. Inclusion: 60 women undergoing breast cancer surgery. Exclusion: Dementia or cognitive impairment that makes it impossible to participate in the study. Arterial blood gas and lung function are undertaken before surgery and the day after surgery

Detailed description

Postoperative hypoxia complicates 30% - 50% of abdominal surgeries. People at particular risk for postoperative pulmonary complications including severe hypoxia are those who undergo abdominal surgery, emergency surgery or have a respiratory failure due to chronic lung disease. The cause of postoperative hypoxia and reduced lung function is unknown. Previous studies report that arterial partial pressure (PaO2) decreased by an average of 2 kilopascal after abdominal surgery, while carbon dioxide partial pressure (PaCO2) was unchanged and vital capacity decreased by 35%. The effect of breast cancer surgery on oxygen and carbon dioxide partial pressure and lung function has to the best of the investigators knowledge not been investigated. This study aims to investigate possible changes in oxygen partial pressure, carbon-dioxide partial pressure and vital capacity after breast cancer surgery. Design: Prospective cohort study participate in studies. Method: Blood gas measurements and Lung function (Vital capacity and FEV1) The day before surgery, the day after surgery and at follow-up. Power analysis: There is a need to investigate 27 patients if the mean (SD) difference is 0.5 (1) kilopascal. Due to drop-outs the investigators calculate a need to include up to 60 patients.

Interventions

None listed

Sponsors

Umeå University
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

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

Inclusion criteria

• Women scheduled for surgery because of breast cancer.

Exclusion criteria

• Dementia or cognitive impairment that makes it impossible to participate in the study.

Design outcomes

Primary

MeasureTime frameDescription
Oxygen partial pressure1 dayChange in oxygen partial pressure after surgery

Secondary

MeasureTime frameDescription
Carbon dioxide partial pressure1 dayChange in carbon dioxide partial pressure after surgery
Vital capacity1 dayChange in vital capacity after surgery
Forced expiratory volume in 1 second (FEV1)1 dayChange in FEV1 after surgery

Countries

Sweden

Contacts

Primary ContactKarl A Franklin, MD, Prof
karl.franklin@umu.se+46 70 6884745
Backup ContactMagnus Hultin, MD, Ass Prof
magnus.hultin@umu.se+46 70 3505335

Outcome results

None listed

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