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。
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:
- Sociodemographic factors (ethnicity, age, sex, body weight, BMI, blood pressure)
- Headache related parameters (onset, duration, pain scale, current medication for headache, menstrual cycle)
- Anxiety, evaluate by Hospital Anxiety and Depression Scale (HADS)
- Depression, evaluate by Beck's Depression Inventory
- Quality of life, evaluate by 36-Item Short Form Survey (SF-36)
- Quality of sleep, evaluate by Pittsburgh Sleep Quality Index (PSQI)
- Aura of headache
- Episodic or chronic headache (If patient diagnosed as migraine.)
- 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:
- Sociodemographic factors (ethnicity, age, sex, body weight, BMI, blood pressure)
- Headache related parameters (onset, duration, pain scale, current medication for headache, menstrual cycle)
- Anxiety, evaluate by Hospital Anxiety and Depression Scale (HADS)
- Depression, evaluate by Beck's Depression Inventory
- Quality of life, evaluate by 36-Item Short Form Survey (SF-36)
- Quality of sleep, evaluate by Pittsburgh Sleep Quality Index (PSQI)
- Aura of headache
- Episodic or chronic headache (If patient diagnosed as migraine.)
- 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
注册 (估计的)
阶段
- 不适用
联系人和位置
学习联系方式
- 姓名:Yuan-Chen Liu, M.D.
- 电话号码:886-972199271
- 邮箱:jordan810701@gmail.com
研究联系人备份
- 姓名:Ching-Chun Chung, M.D.
- 电话号码:886-988566621
- 邮箱:gracechung1015@gmail.com
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
资格标准
适合学习的年龄
接受健康志愿者
有资格学习的性别
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
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
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
研究主要日期
学习开始 (实际的)
初级完成 (估计的)
研究完成 (估计的)
研究注册日期
首次提交
首先提交符合 QC 标准的
首次发布 (实际的)
研究记录更新
最后更新发布 (实际的)
上次提交的符合 QC 标准的更新
最后验证
更多信息
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