Gynecological cancers, including those affecting the ovaries, uterus, and cervix, represent a significant health burden for women. While survival rates have improved, many women experience chronic pelvic pain secondary to cancer treatment, especially radiotherapy and chemotherapy. This treatment-induced pelvic pain can be of difficult management and significantly affects patients' quality of life. In our experience, ozone therapy has emerged as a promising complementary treatment for pain relief in patients with chronic diseases, including side effects of cancer treatment. However, the genetic and epigenetic mechanisms influencing its effectiveness have not yet been thoroughly studied. The aim of this prospective study is to analyze how ozone therapy modulates the expression of certain genes and its impact on epigenetic clocks, which could help predict pain response.
While survival rates of gynecological cancers have improved, many women experience chronic pelvic pain as a consequence of cancer treatment, particularly radiotherapy and chemotherapy. This persistent pain often has neuropathic characteristics, and it can be challenging to manage, negatively impacting physical and emotional well-being and quality of life. Conventional pain management strategies for these patients often provide limited relief. In our experience, ozone therapy has emerged as a promising option for managing chronic pain in various conditions, including side effects of cancer treatment. While the clinical benefits of ozone therapy have been observed in preliminary studies, the underlying molecular mechanisms underlying its analgesic effect remain largely unknown. Understanding how ozone therapy influences gene expression and epigenetic modifications could facilitate the identification of genes involved in the differential response to ozone therapy and a potential way for personalized strategies for pain treatment. The aim of this prospective study is to analyze how ozone therapy modulates the expression of certain genes and its impact on epigenetic clocks, which could help predict pain response. Primary Objectives: In patients with gynecological tumors treated by radiotherapy/chemotherapy, To evaluate * among patients with or without chronic pelvic pain induced by treatment. * before and after ozone treatment in those patients treated because of pelvic pain induced by radiotherapy/chemotherapy. The potential differences in: 1. Gene expression. 2. Biological age based on epigenetic clocks: Secondary Objectives: Evaluate in those patients the potential relationship between gene expression and epigenetic clocks with: 1. Grade of toxicity 2. Pain score 3. Health-related quality of life, 4. Biochemical markers of oxidative stress and inflammation. Trial Design: This observational and prospective study will analyze data from two groups of patients with gynecological tumors treated with radiotherapy/chemotherapy: * A group of patients with chronic pelvic pain secondary to radiotherapy-chemotherapy, submitted to our Chronic Pain Unit for compassionate/palliative ozone treatment. * A group of patients without secondary chronic pelvic pain. Trial Population: Adult women (≥ 18 years old) with gynecological tumors treated with radiotherapy-chemotherapy. They will be analyzed into two different groups of patients: * A group of patients with chronic pelvic pain secondary to radiotherapy-chemotherapy, submitted to our Chronic Pain Unit for compassionate/palliative ozone treatment. * A group of patients without secondary chronic pelvic pain. Intervention. No intervention. The management of patients will be the standard of care in our hospital. Study Duration: The primary completion date is planned for 14/February/2027. The study completion date is planned for 14/August/2027
Study Type
OBSERVATIONAL
Enrollment
40
Hospital Universitario de Gran Canaria Dr. Negrín, (FIISC)
Las Palmas, Las Palmas, Spain
RECRUITINGDifferences in gene expression among patients with or without chronic pelvic pain induced by radiotherapy/chemotherapy.
Differences (among patients with or without chronic pelvic pain induced by radiotherapy/chemotherapy) in gene expression profile.
Time frame: At 0 week
Changes (from baseline) in gene expression at the end of ozone treatment.
Changes (from baseline) in gene expression profile, after ozone treatment.
Time frame: At 16 weeks
Differences in biological age based on epigenetic clocks among patients with or without chronic pelvic pain induced by radiotherapy/chemotherapy
Differences (among patients with or without chronic pain induced by radiotherapy/chemotherapy) in the biological age based on epigenetic clocks.
Time frame: At 0 week.
Changes (from baseline) in the biological age based on epigenetic clocks, after ozone treatment
Changes (from baseline) in the biological age based on epigenetic clocks, after ozone treatment
Time frame: At 16 weeks.
Differences in the grade of toxicity according to the Common Terminology Criteria for Adverse Events (CTCAE) v.5.0 scale among patients with or without chronic pain induced by radiotherapy/chemotherapy
Differences (among patients with or without chronic pain induced by radiotherapy/chemotherapy) in the grade of toxicity according to the Common Terminology Criteria for Adverse Events (CTCAE) v.5.0 scale (from the National Cancer Institute of EEUU). Range from: Grade = (asymptomatic or mild symptoms) to Grade 3 (severe symptoms, limiting self-care activities in daily life).
Time frame: At 0 week.
Changes (from baseline) in the grade of toxicity according to the Common Terminology Criteria for Adverse Events (CTCAE) v.5.0 scale, after ozone treatment.
Changes (from baseline) in the grade of toxicity according to the Common Terminology Criteria for Adverse Events (CTCAE) v.5.0 scale (from the National Cancer Institute of EEUU). Range from: Grade = (asymptomatic or mild symptoms) to Grade 3 (severe symptoms, limiting self-care activities in daily life).
Time frame: At 16 weeks.
Differences in pain score according to the visual analog scale (VAS) among patients with or without chronic pain induced by radiotherapy/chemotherapy
Self-reported evaluation of the severity of pain according to the VAS, scored from 0 ("No pain") to 10 ("Pain as bad as you can imagine").
Time frame: At 0 week.
Change (from baseline) in pain score according to the visual analog scale (VAS), after ozone treatment.
Self-reported evaluation of the severity of pain according to the VAS, scored from 0 ("No pain") to 10 ("Pain as bad as you can imagine").
Time frame: At 16 weeks.
Differences in "Quality of Life" (using the EQ-5D-5L questionnaire) self-perceived by patients among patients with or without chronic pain induced by radiotherapy/chemotherapy.
Self-reported evaluation of: a) 5 physical and emotional items scored in five levels, from 1 (Best: I have no problem) to 5 (worst: I have an extreme problem or I am unable to…) and b) additional self-assessment of health by a visual analog scale (0 = worst health patient can imagine, 100 = best health patient can imagine).
Time frame: At 0 week.
Changes (from baseline) in "Quality of Life" (using the EQ-5D-5L questionnaire) self-perceived by patients, after ozone treatment.
Self-reported evaluation of: a) 5 physical and emotional items scored in five levels, from 1 (Best: I have no problem) to 5 (worst: I have an extreme problem or I am unable to…) and b) additional self-assessment of health by a visual analog scale (0 = worst health patient can imagine, 100 = best health patient can imagine).
Time frame: At 16 weeks.
Differences in biochemical parameters of oxidative stress among patients with or without chronic pain induced by radiotherapy/chemotherapy.
Differences in serum levels of antioxidants and free radicals.
Time frame: At 0 week.
Changes (from baseline) in biochemical parameters of oxidative stress, after ozone treatment.
Changes in serum levels of antioxidants and free radicals.
Time frame: At 16 weeks.
Differences in biochemical parameters of inflammation among patients with or without chronic pain induced by radiotherapy/chemotherapy.
Differences in serum levels of pro-inflammatory cytokines.
Time frame: At 0 week.
Changes (from baseline) in biochemical parameters of inflammation, after ozone treatment.
Changes in serum levels of pro-inflammatory cytokines.
Time frame: At 16 weeks.
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