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偏头痛接受激光针灸与 MMP2 和 CGRP 血液检测的比较:单盲随机对照试验。

2026年9月29日 更新者:Taichung Veterans General Hospital

MMP2 和 CGRP 血液检测中原发性头痛的比较:单盲随机假激光针灸对照研究。

Aims:

To investigate the efficacy of laser-acupuncture for the severity of primary headache and comorbidities, and the Lab data examination.

Methods:

In this hospital-based prospective single blind randomized sham-controlled study, patients over 18 years old with primary headache will be randomly divided into two treatment arms including laser-acupuncture and sham-controlled group. The expected laser-acupuncture protocol will be bilateral BL2, GB20, EX-HN5, GB8, LI4, LR3 and midline EX-HN3 in totally eight sessions at the first month. In the sham-laser-acupuncture group, patients will receive eight sessions of laser-acupuncture for free after unblinding. We expected to track patients for at least half year. The diagnosis and classification of headache was evaluated using the ICHD-3 criteria. The severity of headache was evaluated using Migraine Disability Assessment (MIDAS) and headache diary provided by Taiwan Headache Society. The co-primary efficacy end points are change in migraine days per month and variation of MIDAS. The secondary end point is the reducing of the severity of comorbidities including headache related anxiety and depression, and both of the quality of life and sleep.

In addition, patients' characteristics will be investigated as follows:

  1. Sociodemographic factors (ethnicity, age, sex, body weight, BMI, blood pressure)
  2. Headache related parameters (onset, duration, pain scale, current medication for headache, menstrual cycle)
  3. Anxiety, evaluate by Hospital Anxiety and Depression Scale (HADS)
  4. Depression, evaluate by Beck's Depression Inventory
  5. Quality of life, evaluate by 36-Item Short Form Survey (SF-36)
  6. Quality of sleep, evaluate by Pittsburgh Sleep Quality Index (PSQI)
  7. Aura of headache
  8. Episodic or chronic headache (If patient diagnosed as migraine.)
  9. Nausea, vomiting, photophobia, phonophobia (If patient diagnosed as migraine.) During the following time, we will need the patient's blood samples four times, each times 20cc, all need 80cc for Lab test of MMP2, CGRP, substance P, beta-endorphin.

Importance:

In our hospital, we perform laser-acupuncture for patients with headache for several years. A prospective randomized controlled study is the key tools to establish the efficacy of laser-acupuncture for primary headache, and the Lab data with MMP2, CGRP, substance P, beta-endorphin for approval. Look forward to help improve therapeutic strategies in clinical practice.

研究概览

详细说明

Headache is one of the most common complaints encountered in medical institution as known as an almost universal human experience. Approximately 65% of headaches are classified as primary, which was a composite of migraine, tension-type headache, trigeminal autonomic cephalalgia and other primary headaches according to the third edition of the International Classification of Headache Disorders (ICHD-3). Primary headaches encompass a heterogeneous group of neurologic disorders and might be bothersome for patients.

It's well established that acupuncture can be considered a treatment option for migraine prevention. The efficacy of laser-acupuncture is similar to acupuncture, and laser-acupuncture is a non-invasive therapeutic approach and safety. It could reduce the risk of hemorrhage, infection and needle phobia. However, the efficacy of laser-acupuncture in primary headache remains inconclusive.

MMP2, CGRP, substance P, beta-endorphin are new Lab examination for following up the patients suffered from migraine.

Aims:

To investigate the efficacy of laser-acupuncture for the severity of primary headache and comorbidities, and the Lab data examination.

Methods:

In this hospital-based prospective single blind randomized sham-controlled study, patients over 18 years old with primary headache will be randomly divided into two treatment arms including laser-acupuncture and sham-controlled group. The expected laser-acupuncture protocol will be bilateral BL2, GB20, EX-HN5, GB8, LI4, LR3 and midline EX-HN3 in totally eight sessions at the first month. In the sham-laser-acupuncture group, patients will receive eight sessions of laser-acupuncture for free after unblinding. We expected to track patients for at least half year. The diagnosis and classification of headache was evaluated using the ICHD-3 criteria. The severity of headache was evaluated using Migraine Disability Assessment (MIDAS) and headache diary provided by Taiwan Headache Society. The co-primary efficacy end points are change in migraine days per month and variation of MIDAS. The secondary end point is the reducing of the severity of comorbidities including headache related anxiety and depression, and both of the quality of life and sleep.

In addition, patients' characteristics will be investigated as follows:

  1. Sociodemographic factors (ethnicity, age, sex, body weight, BMI, blood pressure)
  2. Headache related parameters (onset, duration, pain scale, current medication for headache, menstrual cycle)
  3. Anxiety, evaluate by Hospital Anxiety and Depression Scale (HADS)
  4. Depression, evaluate by Beck's Depression Inventory
  5. Quality of life, evaluate by 36-Item Short Form Survey (SF-36)
  6. Quality of sleep, evaluate by Pittsburgh Sleep Quality Index (PSQI)
  7. Aura of headache
  8. Episodic or chronic headache (If patient diagnosed as migraine.)
  9. Nausea, vomiting, photophobia, phonophobia (If patient diagnosed as migraine.) During the following time, we will need the patient's blood samples four times, each times 20cc, all need 80cc for Lab test of MMP2, CGRP, substance P, beta-endorphin.

Importance:

In our hospital, we perform laser-acupuncture for patients with headache for several years. A prospective randomized controlled study is the key tools to establish the efficacy of laser-acupuncture for primary headache, and the Lab data with MMP2, CGRP, substance P, beta-endorphin for approval. Look forward to help improve therapeutic strategies in clinical practice.

研究类型

介入性

注册 (估计的)

60

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。

学习联系方式

研究联系人备份

学习地点

    • Taichang
      • Taichung、Taichang、台湾、404
        • 招聘中
        • Taichung Veterans General Hospital
        • 接触:
          • Yuan-Chen Liu
          • 电话号码:82641 886-4-2359-2525

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

18年 及以上 (成人、年长者)

接受健康志愿者

不

有资格学习的性别

全部

描述

Inclusion Criteria:

  • Migraine patient under the diagnosis and classification of headache was evaluated using the ICHD-3 criteria.

Exclusion Criteria:

  • Age under 18 years old
  • Pregnancy

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:交叉作业
  • 屏蔽:三倍

武器和干预

参与者组/臂
干预/治疗
实验性的:Laser treatment

CM patients with unsatisfactory pharmacological effects receive laser acupuncture for 8 sessions that spanned 4 weeks. Laser stimulation energy of 4.5 J for 30 seconds at each of the following acupoints: bilateral Cuanzhu (BL2), Fengchi (GB20), Taiyang (EX-HN5), Shuaigu (GB8), Hegu (LI4), Taichong (LR3) and midline Yintang (EX-HN3)

Laser stimulation energy of 4.5 J for 30 seconds at each of the following acupoints: bilateral Cuanzhu (BL2), Fengchi (GB20), Taiyang (EX-HN5), Shuaigu (GB8), Hegu (LI4), Taichong (LR3) and midline Yintang (EX-HN3)

假比较器:Sham treatment

CM patients with unsatisfactory pharmacological effects receive sham treatment for 8 sessions that spanned 4 weeks. Sham treatment had no laser output.

Sham treatment with no laser output, stimulate the same acupoints as laser acupuncture group as follows: 30 seconds at bilateral Cuanzhu (BL2), Fengchi (GB20), Taiyang (EX-HN5), Shuaigu (GB8), Hegu (LI4), Taichong (LR3) and midline Yintang (EX-HN3)

After 6 months followed up, the sham group received truely Laser stimulation energy of 4.5 J for 30 seconds at each of the following acupoints: bilateral Cuanzhu (BL2), Fengchi (GB20), Taiyang (EX-HN5), Shuaigu (GB8), Hegu (LI4), Taichong (LR3) and midline Yintang (EX-HN3), and followed up for another 3 months.

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
cGRP
大体时间:12 weeks, 24 weeks, 36 weeks

change in cGRP from baasline and each follow-up time point

12 weeks, 24 weeks, 36 weeks
MMP2
大体时间:12 weeks, 24 weeks, 36 weeks

change in MMP2 from baasline and each follow-up time point

12 weeks, 24 weeks, 36 weeks

次要结果测量

结果测量
措施说明
大体时间
Difference in the number of headache days per month
大体时间:12 weeks, 24 weeks, 36 weeks

change in monthly migraine days (MMD) from baseline and each follow-up time point

12 weeks, 24 weeks, 36 weeks
Difference in the of headache attacks lasting hours per month
大体时间:12 weeks, 24 weeks, 36 weeks

change in acute headache medications usage days per month from baseline and each follow-up time point

12 weeks, 24 weeks, 36 weeks
Difference in the headache pain intensity (NRS)
大体时间:12 weeks, 24 weeks, 36 weeks

changes in the headache severity (based on NRS) between baseline and each follow-up time point

12 weeks, 24 weeks, 36 weeks
Difference in the number of days with acute headache medication intake per month
大体时间:12 weeks, 24 weeks, 36 weeks

change in acute headache medications usage days per month from baseline and each follow-up time point

12 weeks, 24 weeks, 36 weeks
Difference in the Migraine Disability Assessment
大体时间:12 weeks, 24 weeks, 36 weeks

changes in the Migraine Disability Assessmen between baseline and each follow-up time point.

Title: Migraine Disability Assessmen Maximum value:450 Minimum value:0 Higher scores mean: worsen outcome

12 weeks, 24 weeks, 36 weeks
Difference in the Beck's Depression Inventory
大体时间:12 weeks, 24 weeks, 36 weeks

change in Beck's Depression Inventory between baseline and each follow-up time point

Title:Beck's Depression Inventory Maximum value:63 Minimum value:0 Higher scores mean: worsen outcome

12 weeks, 24 weeks, 36 weeks
Difference in the Hospital Anxiety and Depression Scale
大体时间:12 weeks, 24 weeks, 36 weeks

change in Hospital Anxiety and Depression Scale between baseline and each follow-up time point

Title:Hospital Anxiety and Depression Scale Maximum value:21/21 Minimum value:0/0 Higher scores mean:worsen outcome

12 weeks, 24 weeks, 36 weeks
30% reduction in migraine days
大体时间:12 weeks, 24 weeks, 36 weeks

≥ 30% reduction in migraine days between baseline and each follow-up time point

12 weeks, 24 weeks, 36 weeks
Substance P
大体时间:12 weeks, 24 weeks, 36 weeks

change in Substance P from baasline and each follow-up time point

12 weeks, 24 weeks, 36 weeks
beta-endorphin
大体时间:12 weeks, 24 weeks, 36 weeks

change in beta-endorphin from baasline and each follow-up time point

12 weeks, 24 weeks, 36 weeks

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。

调查人员

  • 首席研究员:Chi-Hsiang Chou, M.D.、Taichung Veterans General Hospital
  • 研究主任:Chi Sheng Wang, M.D.、Taichung Veterans General Hospital
  • 研究主任:Huan Yun Wu, M.D.、Taichung Veterans General Hospital

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)

2025年4月7日

初级完成 (估计的)

2027年11月1日

研究完成 (估计的)

2027年12月1日

研究注册日期

首次提交

2024年9月2日

首先提交符合 QC 标准的

2024年9月2日

首次发布 (实际的)

2024年9月4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29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

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.

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