About this trial
Colorectal cancer (CRC) patients undergoing chemotherapy often experience anemia, oxidative stress, and immune suppression, significantly impacting their quality of life and treatment outcomes. Normobaric oxygen (NBO) therapy, which delivers oxygen at atmospheric pressure with elevated oxygen concentration, has shown a potential to enhance erythropoiesis, reduce oxidative stress, and modulate immune function. However, its efficacy in CRC patients remains underexplored. This study aims to evaluate the effects of NBO exposures on (1) supporting erythropoiesis by measuring erythropoietin (EPO) levels and hypoxia-inducible factors (HIF-1α), (2) reducing oxidative stress and improving stress and emotional well-being, and (3) modulating immune function by assessing cytokine profiles. Secondary objectives include assessing the impact of NBO on patient-reported outcome measures (PROMs) such as stress, anxiety, depression, and quality of life. This is a prospective, randomized, double-blind, placebo-controlled clinical trial. A total of 254 CRC patients undergoing chemotherapy will be randomized 1:1 to receive either active NBO therapy (n=127) or placebo NBO therapy (n=127). The intervention consists of 10 NBO sessions over five weeks. Primary outcomes include biomarkers of erythropoiesis, oxidative stress, and immune response. Secondary outcomes assess quality of life and psychological well-being. Data will be collected at baseline, mid-intervention, post-intervention, and during two follow-up visits (3- and 6-months post-intervention). The study hypothesizes that NBO therapy will improve erythropoiesis, reduce oxidative stress, and enhance immune function in CRC patients, leading to improved quality of life and clinical outcomes. Findings from this trial may establish NBO as a novel supportive therapy for CRC patients undergoing chemotherapy.
Eligibility criteria
Qualifiers
age between 18 and 80 years (participants must be adults)
diagnosed with CRC (stage II-IV, scheduled for standard chemotherapy (for study and control groups)
baseline hemoglobin levels above 10 g/dL
no concurrent hematologic malignancies
Disqualifiers
age under 18 years or over 80 years
severe cardiovascular or respiratory conditions (e.g., unstable angina, recent myocardial infarction, advanced COPD)
severe anemia (hemoglobin <10 g/dL) or any hemolytic disorder that could confound study outcomes
uncontrolled diabetes mellitus (e.g., HbA1c >8.0% or poor glycemic control requiring frequent hospitalizations)
Trial design
Treatments tested in this trial
- Normobaric oxygen therapy
- Normobaric oxygen therapy
Treatment groups
Sponsors and collaborators
4th Military Clinical Hospital with Polyclinic, Poland
Lead sponsor
Wroclaw Medical University
Collaborator
Wroclaw University of Science and Technology (Poland)
Collaborator
Hirszfeld Institute of Immunology and Experimental Therapy, Polish Academy of Sciences (Poland)
Collaborator
WSB Merito University in Opole (Poland)
Collaborator
Academy of Applied Sciences in Nowy Sacz (Poland)
Collaborator