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

2026년 9월 25일 업데이트: 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.

연구 개요

상태

완전한

정황

개입 / 치료

상세 설명

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.

연구 유형

중재적

등록 (실제)

66

단계

  • 해당 없음

연락처 및 위치

이 섹션에서는 연구를 수행하는 사람들의 연락처 정보와 이 연구가 수행되는 장소에 대한 정보를 제공합니다.

연구 장소

    • Cairo Governorate
      • Cairo, Cairo Governorate, 이집트, 11771
        • Kobri El Koba Military Hospital

참여기준

연구원은 적격성 기준이라는 특정 설명에 맞는 사람을 찾습니다. 이러한 기준의 몇 가지 예는 개인의 일반적인 건강 상태 또는 이전 치료입니다.

자격 기준

공부할 수 있는 나이

45년 (성인)

건강한 자원 봉사자를 받아들입니다

아니

연구 대상 성별

모두

설명

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).

공부 계획

이 섹션에서는 연구 설계 방법과 연구가 측정하는 내용을 포함하여 연구 계획에 대한 세부 정보를 제공합니다.

연구는 어떻게 설계됩니까?

디자인 세부사항

  • 주 목적: 치료
  • 할당: 무작위
  • 중재 모델: 병렬 할당
  • 마스킹: 없음(오픈 라벨)

무기와 개입

참가자 그룹 / 팔
개입 / 치료
활성 비교기: 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)

실험적: 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.

다른 이름들:
  • HPOT
실험적: 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.

다른 이름들:
  • HPLT

연구는 무엇을 측정합니까?

주요 결과 측정

결과 측정
측정값 설명
기간
Change in Michigan Neuropathy Screening Instrument (MNSI) score
기간: 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
기간: 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
기간: 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
기간: 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
기간: 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
기간: 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
기간: 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
기간: 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
기간: 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
기간: 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
기간: 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
기간: 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
기간: 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

공동 작업자 및 조사자

여기에서 이 연구와 관련된 사람과 조직을 찾을 수 있습니다.

스폰서

연구 기록 날짜

이 날짜는 ClinicalTrials.gov에 대한 연구 기록 및 요약 결과 제출의 진행 상황을 추적합니다. 연구 기록 및 보고된 결과는 공개 웹사이트에 게시되기 전에 특정 품질 관리 기준을 충족하는지 확인하기 위해 국립 의학 도서관(NLM)에서 검토합니다.

연구 주요 날짜

연구 시작 (실제)

2024년 7월 1일

기본 완료 (실제)

2025년 7월 6일

연구 완료 (실제)

2025년 7월 6일

연구 등록 날짜

최초 제출

2026년 8월 31일

QC 기준을 충족하는 최초 제출

2026년 9월 25일

처음 게시됨 (실제)

2026년 9월 30일

연구 기록 업데이트

마지막 업데이트 게시됨 (실제)

2026년 9월 30일

QC 기준을 충족하는 마지막 업데이트 제출

2026년 9월 25일

마지막으로 확인됨

2026년 9월 1일

추가 정보

이 연구와 관련된 용어

기타 연구 ID 번호

  • P.T.REC/012/005181

개별 참가자 데이터(IPD) 계획

개별 참가자 데이터(IPD)를 공유할 계획입니까?

아니요

IPD 계획 설명

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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