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Study of Key Electro-acupuncture Technique on Migraine

Study of Key Electro-acupuncture Technique on Migraine

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02580968
Enrollment
2
Registered
2015-10-20
Start date
2015-03-31
Completion date
2017-12-31
Last updated
2020-02-05

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Migraine

Keywords

Electroacupuncture therapy, Migraine, Acupuncture Therapy

Brief summary

A random controlled trail to evaluate the efficacy of migraine standard electroacupuncture formula, and to analysis the regulation of the intensity-effects and to observe the peripheral NO, CGRP and NF-кB expression level of migraine patients after electroacupuncture treatment.

Detailed description

acupuncture group(group A): treated by acupuncture for 20 days, 1 time per day control group(group B): treated by FlunarizineHydrochloride for 20 days, 1 table per day.

Interventions

DEVICEelectro-acupuncture

electro-acupuncture on acupoints according to the traditional syndrome diagnosis.once per day, for 20 days.

flunarizine hydrochloride ,10mg/day,for 20 days。

Sponsors

Shanghai University of Traditional Chinese Medicine
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* met the diagnostic criteria for migraine; suffering from migraine attacks; migraine attacks for more than 5 days per month, and lasts for 3 months; voluntarily join this study with informed consents.

Exclusion criteria

* other systemic, neurological and psychiatric disorders; headache caused by other diseases; not treatment compliance during the study.

Design outcomes

Primary

MeasureTime frameDescription
Migraine Disability Assessment Questionnaire (MIDAS)20 daysa scientifically reliable and valid measure of migraine disability that can improve communication between patients and physicians, assess migraine severity and act as an outcome measure to monitor treatment efficacy

Secondary

MeasureTime frameDescription
The medical outcomes study 36-item short-form health survey(SF-36)20 daysA 36-item short-form (SF-36) was constructed to survey health status in the Medical Outcomes Study
peripheral Nitrogen Monoxide(NO) protein expression20 daysmarker
peripheral Calcitonin gene related peptide(CGRP) protein expression20 daysmarker
peripheral Nuclear factor-kappa B(NF-кB) protein expression20 daysmarker
Visual Analogue Scale (VAS) to assess pain20 daysVisual Analogue Scale (VAS) were applied to measure pain in patients

Countries

China

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 2, 2026