此页面是自动翻译的,不保证翻译的准确性。请参阅 英文版 对于源文本。

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.

研究概览

详细说明

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.

研究类型

介入性

注册 (实际的)

66

阶段

  • 不适用

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习地点

    • Cairo Governorate
      • Cairo、Cairo Governorate、埃及、11771
        • Kobri El Koba Military Hospital

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

45年 至 60年 (成人)

接受健康志愿者

不

有资格学习的性别

全部

描述

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).

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

研究是如何设计的?

设计细节

  • 主要用途:治疗
  • 分配:随机化
  • 介入模型:并行分配
  • 屏蔽:无(打开标签)

武器和干预

参与者组/臂
干预/治疗
有源比较器: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)

实验性的: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.

其他名称:
  • HPOT
实验性的: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.

其他名称:
  • HPLT

研究衡量的是什么?

主要结果指标

结果测量
措施说明
大体时间
Change in Michigan Neuropathy Screening Instrument (MNSI) score
大体时间: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
大体时间: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
大体时间: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
大体时间: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
大体时间: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
大体时间: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
大体时间: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
大体时间: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
大体时间: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
大体时间: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
大体时间: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
大体时间: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
大体时间: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

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始 (实际的)

2024年7月1日

初级完成 (实际的)

2025年7月6日

研究完成 (实际的)

2025年7月6日

研究注册日期

首次提交

2026年8月31日

首先提交符合 QC 标准的

2026年9月25日

首次发布 (实际的)

2026年9月30日

研究记录更新

最后更新发布 (实际的)

2026年9月30日

上次提交的符合 QC 标准的更新

2026年9月25日

最后验证

2026年9月1日

更多信息

与本研究相关的术语

计划个人参与者数据 (IPD)

计划共享个人参与者数据 (IPD)?

不

IPD 计划说明

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

药物和器械信息、研究文件

研究美国 FDA 监管的药品

不

研究美国 FDA 监管的设备产品

不

此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.

订阅