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Hyperbaric Oxygen Therapy Versus High Power Laser for Diabetic Neuropathy (HBOT-HPLT-DPN)

2026年9月25日 更新者:Mostafa Mahmoud Mohamed Youssef Khalifa、Cairo University

Hyperbaric Oxygen Therapy Versus High Power Laser Therapy On Sensorimotor Functions In Patients With Diabetic Peripheral Neuropathy

The purpose of this study is to compare the clinical effects of Hyperbaric Oxygen Therapy (HBOT) versus High-Intensity Laser Therapy (HPLT) on sensorimotor functions and nerve conduction in patients suffering from painful diabetic peripheral neuropathy.

Participants are divided into three equal groups. The first group receives a traditional physiotherapy program focused on ankle and foot exercises. The second group receives hyperbaric oxygen therapy sessions in addition to the traditional program. The third group receives high-power MLS laser therapy alongside the traditional program. Investigators look at whether either advanced intervention shows superiority in improving nerve functionality and reducing neuropathic pain.

調査の概要

詳細な説明

Diabetic peripheral neuropathy (DPN) is a major microvascular complication of diabetes leading to progressive nerve damage and neuropathic pain. This randomized controlled trial evaluates and compares the efficacy of two non-pharmacological interventions: Hyperbaric Oxygen Therapy (HBOT) and High-Intensity Laser Therapy (HPLT).

A total of 66 medically controlled patients with painful diabetic neuropathy are randomly assigned into three equal parallel groups (22 patients per group):

  • Control Group (A): Receives a traditional physiotherapy program including foot and ankle ROM exercises, strengthening, and functional walking training for 5 sessions per week for 3 weeks.
  • Study Group (B): Receives Hyperbaric Oxygen Therapy (100% oxygen at 2.5 ATA for 60 minutes, totaling 90 minutes per session) for 15 sessions over 3 weeks, combined with the traditional physiotherapy program.
  • Study Group (C): Receives High-Power Laser Therapy using a Multiwave Locked System (MLS) laser device (1500 Hz frequency) applied every other day for 9 sessions over 3 weeks, combined with the traditional physiotherapy program.

Assessments are conducted before and after the 3-week treatment period using objective Nerve Conduction Studies (NCS) for the sural and common peroneal nerves, and subjective screening via the Arabic Michigan Neuropathy Screening Instrument (MNSI) score.

研究の種類

介入

入学 (実際)

66

段階

  • 適用できない

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。

研究場所

    • Cairo Governorate
      • Cairo、Cairo Governorate、エジプト、11771
        • Kobri El Koba Military Hospital

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

45年~60年 (大人)

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

全て

説明

Inclusion Criteria:

  • Patients diagnosed with type 2 diabetes mellitus for more than 5 years.
  • Presence of painful diabetic peripheral neuropathy lasting for more than 6 months.
  • Presence of sensory abnormalities, burning pain, and impaired nerve conduction velocity in the lower extremities.
  • Medically controlled glycemic status.
  • Sufficient cognitive abilities with a Mini-Mental State Examination (MMSE) score greater than 24.
  • Fit for hyperbaric pressure therapy with a cardiac ejection fraction (CEF) equal to or greater than 50% and blood pressure equal to or less than 150/90 mmHg.

Exclusion Criteria:

  • Peripheral neuropathy resulting from causes other than diabetes (e.g., vitamin B12 deficiency, alcohol abuse, or trauma).
  • Severe vascular insufficiency in the lower limbs.
  • Uncontrolled medical conditions such as tumors or thyroid dysfunction.
  • Pregnancy.
  • Presence of metallic implantations or cardiac pacemakers.
  • Severe visual, auditory, or cognitive impairment (MMSE score less than 24).
  • Chronic obstructive pulmonary disease (COPD) or other contraindications to hyperbaric oxygen therapy.
  • History of other neurological diseases (e.g., stroke or multiple sclerosis).

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

  • 主な目的:処理
  • 割り当て:ランダム化
  • 介入モデル:並列代入
  • マスキング:なし(オープンラベル)

武器と介入

参加者グループ / アーム
介入・治療
アクティブコンパレータ:Conventional Physiotherapy

Foot and ankle range of motion (ROM) exercises, strengthening exercises, functional exercises, and walking training (5 sessions per week for 3 weeks).

Foot and ankle range of motion (ROM) exercises, strengthening exercises, functional exercises, and walking training (5 sessions per week for 3 weeks)

実験的:Hyperbaric Oxygen Therapy (HBOT)

Conventional physiotherapy program plus HBOT sessions (100% oxygen at 2.5 ATA for 60 minutes, with 15 minutes gradual compression and 15 minutes decompression, totaling 90 minutes per session). 15 sessions over 3 weeks.

100% oxygen inhalation at 2.5 ATA pressure for 60 minutes inside a hyperbaric chamber.

他の名前:
  • HPOT
実験的:High-Power Laser Therapy (HPLT)

Conventional physiotherapy program plus HPLT (MLS laser, M6). Applied every other day for 9 sessions over 3 weeks. Includes a remote foot scan followed by contact application on 7 specific lower extremity areas.

MLS laser (M6 device) at 1500 Hz frequency, applied every other day for 9 sessions over 3 weeks. Includes a remote foot scan followed by contact application on 7 specific lower extremity areas.

他の名前:
  • HPLT

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
Change in Michigan Neuropathy Screening Instrument (MNSI) score
時間枠:Baseline and 3 weeks post-treatment

The Michigan Neuropathy Screening Instrument (MNSI) questionnaire was used to assess symptoms of diabetic peripheral neuropathy. Abnormal responses were summed to obtain the total score. The questionnaire score ranges from 0 to 13, with higher scores indicating greater neuropathic symptom burden.

Baseline and 3 weeks post-treatment
Change in right sural nerve distal sensory latency
時間枠:Baseline and after 3 weeks of treatment

Right sural nerve distal sensory latency was assessed using nerve conduction studies and measured in milliseconds (ms).

Baseline and after 3 weeks of treatment
Change in left sural nerve distal sensory latency
時間枠:Baseline and after 3 weeks of treatment

Left sural nerve distal sensory latency was assessed using nerve conduction studies and measured in milliseconds (ms).

Baseline and after 3 weeks of treatment
Change in right sural nerve sensory amplitude
時間枠:Baseline and after 3 weeks of treatment

Right sural nerve sensory amplitude was assessed using nerve conduction studies and measured in microvolts (µV).

Baseline and after 3 weeks of treatment
Change in left sural nerve sensory amplitude
時間枠:Baseline and after 3 weeks of treatment

Left sural nerve sensory amplitude was assessed using nerve conduction studies and measured in microvolts (µV).

Baseline and after 3 weeks of treatment
Change in right sural nerve conduction velocity
時間枠:Baseline and after 3 weeks of treatment

Right sural nerve conduction velocity was assessed using nerve conduction studies and measured in meters per second (m/s).

Baseline and after 3 weeks of treatment
Change in left sural nerve conduction velocity
時間枠:Baseline and after 3 weeks of treatment

Left sural nerve conduction velocity was assessed using nerve conduction studies and measured in meters per second (m/s).

Baseline and after 3 weeks of treatment
Change in right peroneal nerve distal motor latency
時間枠:Baseline and after 3 weeks of treatment

Right peroneal nerve distal motor latency was assessed using nerve conduction studies and measured in milliseconds (ms).

Baseline and after 3 weeks of treatment
Change in left peroneal nerve distal motor latency
時間枠:Baseline and after 3 weeks of treatment

Left peroneal nerve distal motor latency was assessed using nerve conduction studies and measured in milliseconds (ms).

Baseline and after 3 weeks of treatment
Change in right peroneal nerve motor amplitude
時間枠:Baseline and after 3 weeks of treatment

Right peroneal nerve motor amplitude was assessed using nerve conduction studies and measured in millivolts (mV).

Baseline and after 3 weeks of treatment
Change in left peroneal nerve motor amplitude
時間枠:Baseline and after 3 weeks of treatment

Left peroneal nerve motor amplitude was assessed using nerve conduction studies and measured in millivolts (mV).

Baseline and after 3 weeks of treatment
Change in right peroneal nerve motor conduction velocity
時間枠:Baseline and after 3 weeks of treatment

Right peroneal nerve motor conduction velocity was assessed using nerve conduction studies and measured in meters per second (m/s).

Baseline and after 3 weeks of treatment
Change in left peroneal nerve motor conduction velocit
時間枠:Baseline and after 3 weeks of treatment

Left peroneal nerve motor conduction velocity was assessed using nerve conduction studies and measured in meters per second (m/s).

Baseline and after 3 weeks of treatment

協力者と研究者

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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)

2024年7月1日

一次修了 (実際)

2025年7月6日

研究の完了 (実際)

2025年7月6日

試験登録日

最初に提出

2026年8月31日

QC基準を満たした最初の提出物

2026年9月25日

最初の投稿 (実際)

2026年9月30日

学習記録の更新

投稿された最後の更新 (実際)

2026年9月30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25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?

いいえ

IPD プランの説明

Individual participant data will not be shared outside the research team to maintain patient privacy and data confidentiality in accordance with institutional guidelines.

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