Normobaric Oxygen Therapy in Colorectal Cancer Patients

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-80
Sponsor4th Military Clinical Hospital with Polyclinic, Poland

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

254 Participants
are divided into 2 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