The Efficacy and Safety of Acupuncture for Prophylaxis of Menstrually Related Migraine

NCT ID
NCT07023926
Registry status
Recruiting
Study type
Interventional
Phase
Not applicable
Sponsor
Guang'anmen Hospital of China Academy of Chinese Medical Sciences
Conditions
Electroacupuncture, Menstrually Related Migraine

Overview

ClinicalTrials.gov lists this study as Recruiting.

Official title: The Efficacy and Safety of Acupuncture for Prophylaxis of Menstrually Related Migraine: a Pilot Randomized Controlled Trial

Enrollment: 40 participants (Estimated).

What is being studied

  • Intervention: Acupuncture Therapy
  • Intervention: Analgesia
  • Intervention: Anesthesia
  • Intervention: Anesthesia and Analgesia
  • Intervention: Combined Modality Therapy
  • Intervention: Complementary Therapies
  • Intervention: Electric Stimulation Therapy
  • Device: electroacupuncture
  • Intervention: Electroacupuncture
  • Intervention: Physical Therapy Modalities
  • Intervention: Rehabilitation
  • Device: Sham electroacupuncture
  • Intervention: Therapeutics
  • Intervention: Transcutaneous Electric Nerve Stimulation

Who may be eligible

Ages
18 Years to 45 Years
Sex
Female
Healthy volunteers accepted
No

ClinicalTrials.gov lists the following eligibility criteria.

Inclusion Criteria: 1. meet the diagnostic criteria for MRM according to the ICHD-3, with a documented history of MRM for at least 12 months; 2. have a confirmed diagnosis of migraine by a neurologist; 3. aged 18-45 years; 4. have regular menstrual cycles (28 ± 7 days) with menstruation lasting 3-7 days; 5. have experienced ≥3 headache days during each menstrual cycle (days -2 to +3) and ≥5 total headache days per cycle over the past 3 months and baseline period; migraine attacks must last 4-72 hours without acute medication, or at least 2 hours when treated; 6. have completed a headache diary during the screening period (covering at least one full menstrual cycle), demonstrating good compliance; 7. headache diary data during screening period must meet the ICHD-3 criteria for MRM and fulfill criteria (4) and (5); 8. voluntarily sign the informed consent. Exclusion Criteria: 1. irregular menstrual cycles, defined as cycle length outside the range of 28±7 days or menstruation duration \<3 days or \>7 days; 2. presence of secondary headache disorders, facial neuralgia, or cranial neuralgia; 3. combined with serious primary diseases such as cardiovascular, hepatic, renal, gastrointestinal, or hematological disorders that may interfere with the treatment protocol, or comorbid neurological conditions such as epilepsy, parkinson's disease, or other central nervous system disorders; 4. headache symptoms caused by other conditions, such as moderate to severe head or neck trauma, perimenstrual infections, intracranial tumors, intracranial infections, endocrine or metabolic disorders; 5. receipt of preventive treatment for headache within 1 month prior to the screening visit; 6. afraid of needles or received acupuncture treatment within 3 months; 7. unwillingness to undergo the study intervention or failure to sign the informed consent.

Study locations

1 study location is listed.

Recruiting site status is explicitly provided for 1 location; 1 is listed as Recruiting.

Countries: China

  • Beijing Municipality, China: 1

Sample of listed locations

  • Department of Acupuncture, China Academy of Chinese Medical Sciences Guang'anmen Hospital — Beijing, Beijing Municipality, 100053, China — Recruiting

Study details

Start date
July 1, 2025
Primary completion date
December 31, 2027
Completion date
January 31, 2028
First posted
June 17, 2025

Source and update information

Source
ClinicalTrials.gov
NCT ID
NCT07023926
Registry last updated
September 14, 2026
QualifiedStudies registry data refreshed
October 5, 2026
QualifiedStudies record fetched
October 5, 2026

View NCT07023926 on ClinicalTrials.gov

Trial information can change. Confirm current study details with the study team or the registry.

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