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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)

2026年9月22日 更新者: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.

調査の概要

詳細な説明

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

研究の種類

観察的

入学 (推定)

40

連絡先と場所

このセクションには、調査を実施する担当者の連絡先の詳細と、この調査が実施されている場所に関する情報が記載されています。

研究連絡先

研究連絡先のバックアップ

  • 名前:Francisco Rodríguez-Esparragón, BSc, PhD
  • 電話番号:34928449288
  • メール:afrodesp@gmail.com

研究場所

    • Las Palmas
      • Las Palmas、Las Palmas、スペイン、35019
        • 募集
        • Hospital Universitario de Gran Canaria Dr. Negrín, (FIISC)
        • コンタクト:
        • コンタクト:
          • Francisco Rodríguez-Esparragón, BSc, PhD
          • 電話番号:34928449288
          • メール:afrodesp@gmail.com
        • 主任研究者:
          • Sara Cazorla-Rivero, BSc, PhD
        • 主任研究者:
          • Mario Federico, MD, PhD

参加基準

研究者は、適格基準と呼ばれる特定の説明に適合する人を探します。これらの基準のいくつかの例は、人の一般的な健康状態または以前の治療です。

適格基準

就学可能な年齢

18年歳以上 (大人、高齢者)

健康ボランティアの受け入れ

いいえ

受講資格のある性別

女性

サンプリング方法

非確率サンプル

調査対象母集団

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

説明

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

研究計画

このセクションでは、研究がどのように設計され、研究が何を測定しているかなど、研究計画の詳細を提供します。

研究はどのように設計されていますか?

デザインの詳細

  • 観測モデル:CASE_CONTROL
  • 時間の展望:PROSPECTIVE

コホートと介入

グループ/コホート
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.

この研究は何を測定していますか?

主要な結果の測定

結果測定
メジャーの説明
時間枠
Differences in gene expression among patients with or without chronic pelvic pain induced by radiotherapy/chemotherapy.
時間枠: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.
時間枠: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
時間枠: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
時間枠:At 16 weeks.

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

At 16 weeks.

二次結果の測定

結果測定
メジャーの説明
時間枠
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
時間枠: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.
時間枠: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
時間枠: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.
時間枠: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.
時間枠: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.
時間枠: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.
時間枠: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.
時間枠: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.
時間枠: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.
時間枠:At 16 weeks.

Changes in serum levels of pro-inflammatory cytokines.

At 16 weeks.

協力者と研究者

ここでは、この調査に関係する人々や組織を見つけることができます。

スポンサー

捜査官

  • スタディチェア:Bernardino Clavo, MD, PhD、Hospital Universitario de Gran Canaria Dr. Negrín, (FIISC), Las Palmas, Spain.
  • スタディディレクター:Francisco Rodríguez-Esparragón, BSc, PhD、Hospital Universitario de Gran Canaria Dr. Negrín, (FIISC), Las Palmas, Spain.
  • 主任研究者:Sara Cazorla-Rivero, BSc, PhD、Hospital Universitario de Gran Canaria Dr. Negrín, (FIISC), Las Palmas, Spain.
  • 主任研究者:Mario Federico, MD, PhD、Hospital Universitario de Gran Canaria Dr. Negrín, (FIISC), Las Palmas, Spain.

出版物と役立つリンク

研究に関する情報を入力する責任者は、自発的にこれらの出版物を提供します。これらは、研究に関連するあらゆるものに関するものである可能性があります。

一般刊行物

研究記録日

これらの日付は、ClinicalTrials.gov への研究記録と要約結果の提出の進捗状況を追跡します。研究記録と報告された結果は、国立医学図書館 (NLM) によって審査され、公開 Web サイトに掲載される前に、特定の品質管理基準を満たしていることが確認されます。

主要日程の研究

研究開始 (実際)

2025年2月10日

一次修了 (推定)

2027年2月14日

研究の完了 (推定)

2027年8月14日

試験登録日

最初に提出

2025年2月4日

QC基準を満たした最初の提出物

2025年2月4日

最初の投稿 (実際)

2025年2月10日

学習記録の更新

投稿された最後の更新 (実際)

2026年9月25日

QC基準を満たした最後の更新が送信されました

2026年9月22日

最終確認日

2026年9月1日

詳しくは

本研究に関する用語

個々の参加者データ (IPD) の計画

個々の参加者データ (IPD) を共有する予定はありますか?

はい

IPD プランの説明

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 共有時間枠

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

IPD 共有アクセス基準

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 共有サポート情報タイプ

  • STUDY_PROTOCOL
  • SAP
  • ICF
  • CSR

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