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NCT Number: NCT06584409

Migraines Accepted Laser Acupuncture Compared in Blood Test of MMP2 and CGRP

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.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Taichung Veterans General Hospital

Taichung, Taichang, 404, Taiwan

Location status: Recruiting

Location contact

Yuan-Chen Liu

CONTACT

886-4-2359-2525 ext. 82641

About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

Laser Pen

Device

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)

observation

Other

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.

Primary outcomes

  1. cGRP

    Time frame: 12 weeks, 24 weeks, 36 weeks

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

  2. MMP2

    Time frame: 12 weeks, 24 weeks, 36 weeks

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

Secondary outcomes

  1. Difference in the number of headache days per month

    Time frame: 12 weeks, 24 weeks, 36 weeks

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

  2. Difference in the of headache attacks lasting hours per month

    Time frame: 12 weeks, 24 weeks, 36 weeks

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

  3. Difference in the headache pain intensity (NRS)

    Time frame: 12 weeks, 24 weeks, 36 weeks

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

  4. Difference in the number of days with acute headache medication intake per month

    Time frame: 12 weeks, 24 weeks, 36 weeks

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

  5. Difference in the Migraine Disability Assessment

    Time frame: 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

  6. Difference in the Beck's Depression Inventory

    Time frame: 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

  7. Difference in the Hospital Anxiety and Depression Scale

    Time frame: 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

  8. 30% reduction in migraine days

    Time frame: 12 weeks, 24 weeks, 36 weeks

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

  9. Substance P

    Time frame: 12 weeks, 24 weeks, 36 weeks

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

  10. beta-endorphin

    Time frame: 12 weeks, 24 weeks, 36 weeks

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

Study contacts

Contact information is provided by the study sponsor or research team.

Ching-Chun Chung, M.D.

CONTACT

[email protected]

886-988566621

Yuan-Chen Liu, M.D.

CONTACT

[email protected]

886-972199271

Sponsors and collaborators

Lead sponsor

Taichung Veterans General Hospital

Other

Registry information

Official study title

The Comparsion of Primary Headache in Blood Test of MMP2 and CGRP: A Single Blind Randomized Sham-laser-acupuncture Controlled Study.

Important dates

Study start
2025
Primary completion
2025
Study completion
2027
First posted
Sep 4, 2024
Registry last updated
Apr 8, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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