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Agopuntura laser accettata per l'emicrania rispetto all'esame del sangue di MMP2 e CGRP: un singolo studio randomizzato cieco.

29 settembre 2026 aggiornato da: Taichung Veterans General Hospital

Il confronto tra la cefalea primaria nell'esame del sangue di MMP2 e CGRP: uno studio controllato randomizzato in cieco con agopuntura-laser-sham.

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.

Panoramica dello studio

Stato

Reclutamento

Descrizione dettagliata

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.

Tipo di studio

Interventistico

Iscrizione (Stimato)

60

Fase

  • Non applicabile

Contatti e Sedi

Questa sezione fornisce i recapiti di coloro che conducono lo studio e informazioni su dove viene condotto lo studio.

Contatto studio

Backup dei contatti dello studio

Luoghi di studio

    • Taichang
      • Taichung, Taichang, Taiwan, 404
        • Reclutamento
        • Taichung Veterans General Hospital
        • Contatto:
          • Yuan-Chen Liu
          • Numero di telefono: 82641 886-4-2359-2525

Criteri di partecipazione

I ricercatori cercano persone che corrispondano a una certa descrizione, chiamata criteri di ammissibilità. Alcuni esempi di questi criteri sono le condizioni generali di salute di una persona o trattamenti precedenti.

Criteri di ammissibilità

Età idonea allo studio

18 anni e precedenti (Adulto, Adulto più anziano)

Accetta volontari sani

No

Sessi ammissibili allo studio

Tutto

Descrizione

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

Piano di studio

Questa sezione fornisce i dettagli del piano di studio, compreso il modo in cui lo studio è progettato e ciò che lo studio sta misurando.

Come è strutturato lo studio?

Dettagli di progettazione

  • Scopo principale: Trattamento
  • Assegnazione: Randomizzato
  • Modello interventistico: Assegnazione incrociata
  • Mascheramento: Triplicare

Armi e interventi

Gruppo di partecipanti / Arm
Intervento / Trattamento
Sperimentale: 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)

Comparatore fittizio: 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.

Cosa sta misurando lo studio?

Misure di risultato primarie

Misura del risultato
Misura Descrizione
Lasso di tempo
cGRP
Lasso di tempo: 12 weeks, 24 weeks, 36 weeks

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

12 weeks, 24 weeks, 36 weeks
MMP2
Lasso di tempo: 12 weeks, 24 weeks, 36 weeks

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

12 weeks, 24 weeks, 36 weeks

Misure di risultato secondarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Difference in the number of headache days per month
Lasso di tempo: 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
Lasso di tempo: 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)
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 12 weeks, 24 weeks, 36 weeks

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

12 weeks, 24 weeks, 36 weeks

Collaboratori e investigatori

Qui è dove troverai le persone e le organizzazioni coinvolte in questo studio.

Investigatori

  • Investigatore principale: Chi-Hsiang Chou, M.D., Taichung Veterans General Hospital
  • Direttore dello studio: Chi Sheng Wang, M.D., Taichung Veterans General Hospital
  • Direttore dello studio: Huan Yun Wu, M.D., Taichung Veterans General Hospital

Studiare le date dei record

Queste date tengono traccia dell'avanzamento della registrazione dello studio e dell'invio dei risultati di sintesi a ClinicalTrials.gov. I record degli studi e i risultati riportati vengono esaminati dalla National Library of Medicine (NLM) per assicurarsi che soddisfino specifici standard di controllo della qualità prima di essere pubblicati sul sito Web pubblico.

Studia le date principali

Inizio studio (Effettivo)

7 aprile 2025

Completamento primario (Stimato)

1 novembre 2027

Completamento dello studio (Stimato)

1 dicembre 2027

Date di iscrizione allo studio

Primo inviato

2 settembre 2024

Primo inviato che soddisfa i criteri di controllo qualità

2 settembre 2024

Primo Inserito (Effettivo)

4 settembre 2024

Aggiornamenti dei record di studio

Ultimo aggiornamento pubblicato (Effettivo)

30 settembre 2026

Ultimo aggiornamento inviato che soddisfa i criteri QC

29 settembre 2026

Ultimo verificato

1 settembre 2026

Maggiori informazioni

Termini relativi a questo studio

Piano per i dati dei singoli partecipanti (IPD)

Hai intenzione di condividere i dati dei singoli partecipanti (IPD)?

NO

Informazioni su farmaci e dispositivi, documenti di studio

Studia un prodotto farmaceutico regolamentato dalla FDA degli Stati Uniti

No

Studia un dispositivo regolamentato dalla FDA degli Stati Uniti

No

Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .

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