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Gene and Molecular Pathways of Ozone Treatment Response in Gynecological Tumor Patients With Chronic Pelvic Pain Secondary to Cancer Treatment (OzoGynEpigen)

22. september 2026 opdateret af: Bernardino Clavo, MD, PhD

Gene and Molecular Pathway Characterization of the Response to Ozone Treatment in Gynecological Tumor Patients With Chronic Pelvic Pain Secondary to Radio-chemotherapy

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.

Studieoversigt

Status

Rekruttering

Betingelser

Detaljeret beskrivelse

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

Undersøgelsestype

Observationel

Tilmelding (Anslået)

40

Kontakter og lokationer

Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.

Studiekontakt

Undersøgelse Kontakt Backup

  • Navn: Francisco Rodríguez-Esparragón, BSc, PhD
  • Telefonnummer: 34928449288
  • E-mail: afrodesp@gmail.com

Studiesteder

    • Las Palmas
      • Las Palmas, Las Palmas, Spanien, 35019
        • Rekruttering
        • Hospital Universitario de Gran Canaria Dr. Negrín, (FIISC)
        • Kontakt:
        • Kontakt:
          • Francisco Rodríguez-Esparragón, BSc, PhD
          • Telefonnummer: 34928449288
          • E-mail: afrodesp@gmail.com
        • Ledende efterforsker:
          • Sara Cazorla-Rivero, BSc, PhD
        • Ledende efterforsker:
          • Mario Federico, MD, PhD

Deltagelseskriterier

Forskere leder efter personer, der passer til en bestemt beskrivelse, kaldet berettigelseskriterier. Nogle eksempler på disse kriterier er en persons generelle helbredstilstand eller tidligere behandlinger.

Berettigelseskriterier

Aldre berettiget til at studere

18 år og ældre (Voksen, Ældre voksen)

Tager imod sunde frivillige

Ingen

Køn, der er berettiget til at studere

Kvinde

Prøveudtagningsmetode

Ikke-sandsynlighedsprøve

Studiebefolkning

Adult women (≥18 years) with gynecological tumors treated with radiotherapy-chemotherapy.

Beskrivelse

Inclusion Criteria:

  • Adult women (>=18 years old) with gynecological tumors treated with radiotherapy-chemotherapy.
  • Cancer disease is stable or in remission.
  • Life expectancy > = 6 months.
  • Patients included in the group of patients with pelvic pain must have a clinical, radiological, endoscopic, or histopathological diagnosis that their pain is not secondary to the oncological process.
  • Patients included in the group of patients with pelvic pain must have pain for >= 3 months duration, with an intensity >= 3 on the Visual Analog Scale (VAS), or classified as toxicity >= Grade-2 of the CTCAE v.5.0 of the National Cancer Institute of the USA.
  • Signed and dated informed consent specific to this study.

Exclusion Criteria:

  • Age < 18 years old.
  • Severe psychiatric disorders.
  • Inability to complete the quality of life questionnaires.
  • Active neoplasia requiring recent initiation (< 3 months) of systemic or local treatment.
  • Life expectancy (for any reason) < 6 months.
  • Failure to meet all inclusion criteria

Studieplan

Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.

Hvordan er undersøgelsen tilrettelagt?

Design detaljer

  • Observationsmodeller: CASE_CONTROL
  • Tidsperspektiver: PROSPECTIVE

Kohorter og interventioner

Gruppe / kohorte
Treated patients, without secondary pain

Patients with gynecological tumors, treated with radiotherapy/chemotherapy, without chronic pelvic pain.

Treated patients, with chronic pelvic pain

Patients with gynecological tumors, treated with radiotherapy/chemotherapy, with chronic pelvic pain, submitted to our Chronic Pain Unit for compassionate/palliative ozone treatment.

Hvad måler undersøgelsen?

Primære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
Differences in gene expression among patients with or without chronic pelvic pain induced by radiotherapy/chemotherapy.
Tidsramme: At 0 week

Differences (among patients with or without chronic pelvic pain induced by radiotherapy/chemotherapy) in gene expression profile.

At 0 week
Changes (from baseline) in gene expression at the end of ozone treatment.
Tidsramme: At 16 weeks

Changes (from baseline) in gene expression profile, after ozone treatment.

At 16 weeks
Differences in biological age based on epigenetic clocks among patients with or without chronic pelvic pain induced by radiotherapy/chemotherapy
Tidsramme: At 0 week.

Differences (among patients with or without chronic pain induced by radiotherapy/chemotherapy) in the biological age based on epigenetic clocks.

At 0 week.
Changes (from baseline) in the biological age based on epigenetic clocks, after ozone treatment
Tidsramme: At 16 weeks.

Changes (from baseline) in the biological age based on epigenetic clocks, after ozone treatment

At 16 weeks.

Sekundære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
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
Tidsramme: At 0 week.

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).

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.
Tidsramme: At 16 weeks.

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).

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
Tidsramme: At 0 week.

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").

At 0 week.
Change (from baseline) in pain score according to the visual analog scale (VAS), after ozone treatment.
Tidsramme: At 16 weeks.

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").

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.
Tidsramme: At 0 week.

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).

At 0 week.
Changes (from baseline) in "Quality of Life" (using the EQ-5D-5L questionnaire) self-perceived by patients, after ozone treatment.
Tidsramme: At 16 weeks.

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).

At 16 weeks.
Differences in biochemical parameters of oxidative stress among patients with or without chronic pain induced by radiotherapy/chemotherapy.
Tidsramme: At 0 week.

Differences in serum levels of antioxidants and free radicals.

At 0 week.
Changes (from baseline) in biochemical parameters of oxidative stress, after ozone treatment.
Tidsramme: At 16 weeks.

Changes in serum levels of antioxidants and free radicals.

At 16 weeks.
Differences in biochemical parameters of inflammation among patients with or without chronic pain induced by radiotherapy/chemotherapy.
Tidsramme: At 0 week.

Differences in serum levels of pro-inflammatory cytokines.

At 0 week.
Changes (from baseline) in biochemical parameters of inflammation, after ozone treatment.
Tidsramme: At 16 weeks.

Changes in serum levels of pro-inflammatory cytokines.

At 16 weeks.

Samarbejdspartnere og efterforskere

Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.

Sponsor

Samarbejdspartnere

Efterforskere

  • Studiestol: Bernardino Clavo, MD, PhD, Hospital Universitario de Gran Canaria Dr. Negrín, (FIISC), Las Palmas, Spain.
  • Studieleder: Francisco Rodríguez-Esparragón, BSc, PhD, Hospital Universitario de Gran Canaria Dr. Negrín, (FIISC), Las Palmas, Spain.
  • Ledende efterforsker: Sara Cazorla-Rivero, BSc, PhD, Hospital Universitario de Gran Canaria Dr. Negrín, (FIISC), Las Palmas, Spain.
  • Ledende efterforsker: Mario Federico, MD, PhD, Hospital Universitario de Gran Canaria Dr. Negrín, (FIISC), Las Palmas, Spain.

Publikationer og nyttige links

Den person, der er ansvarlig for at indtaste oplysninger om undersøgelsen, leverer frivilligt disse publikationer. Disse kan handle om alt relateret til undersøgelsen.

Generelle publikationer

Datoer for undersøgelser

Disse datoer sporer fremskridtene for indsendelser af undersøgelsesrekord og resumeresultater til ClinicalTrials.gov. Studieregistreringer og rapporterede resultater gennemgås af National Library of Medicine (NLM) for at sikre, at de opfylder specifikke kvalitetskontrolstandarder, før de offentliggøres på den offentlige hjemmeside.

Studer store datoer

Studiestart (Faktiske)

10. februar 2025

Primær færdiggørelse (Anslået)

14. februar 2027

Studieafslutning (Anslået)

14. august 2027

Datoer for studieregistrering

Først indsendt

4. februar 2025

Først indsendt, der opfyldte QC-kriterier

4. februar 2025

Først opslået (Faktiske)

10. februar 2025

Opdateringer af undersøgelsesjournaler

Sidste opdatering sendt (Faktiske)

25. september 2026

Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier

22. september 2026

Sidst verificeret

1. september 2026

Mere information

Begreber relateret til denne undersøgelse

Andre undersøgelses-id-numre

  • 2024-192-1
  • CIGC'23/24 (Andet bevillings-/finansieringsnummer: Cabildo de Gran Canaria)
  • DISA'24: OA24/104 (Andet bevillings-/finansieringsnummer: Fundación DISA)

Plan for individuelle deltagerdata (IPD)

Planlægger du at dele individuelle deltagerdata (IPD)?

JA

IPD-planbeskrivelse

It will be available (after request):

  • Individual participant data (IPD) that underlie the results reported in further articles, after deidentification
  • Data will be available after publication, ending 36 months following article publication.
  • They will be available for investigators whose proposed use of the data has been approved by an independent review committee identified for this purpose.
  • Study protocol

Proposals should be directed to: bernardinoclavo@gmail.com To gain access, data requestors will need to sign a data access agreement.

IPD-delingstidsramme

Data will be available after publication, ending 36 months following article publication.

IPD-delingsadgangskriterier

Data will be available for investigators whose proposed use of the data has been approved by an independent review committee identified for this purpose.

- Study protocol

Proposals should be directed to: bernardinoclavo@gmail.com To gain access, data requestors will need to sign a data access agreement.

IPD-deling Understøttende informationstype

  • STUDY_PROTOCOL
  • SAP
  • ICF
  • CSR

Lægemiddel- og udstyrsoplysninger, undersøgelsesdokumenter

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