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Clinical Study on the Effects of Female Migraine Without Aura by Opposing Needling

Clinical Study on the Effects of Female Migraine Without Aura by Opposing Needling

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100051479
Enrollment
Unknown
Registered
2021-09-24
Start date
2021-10-01
Completion date
Unknown
Last updated
2022-06-20

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

Conditions

Migraine without aura

Interventions

Experimental group:Contralateral acupuncture
Control group1:ipsilateral acupuncture
Control group 2:Sham contralateral acupuncture

Sponsors

Yunnan University of Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1. Unilateral migraine, women, age is between 18-60 years old (the starting age is less than 50 years old); 2. Meet the ICHD-3 diagnostic criteria for MwoA; 3. In the past 3 months, the number of monthly migraine attacks is greater than or equal to 2 times, and the number of migraine days is less than 15 days per month; 4. The severity of migraine attacks in the past 4 weeks (baseline period) is moderate to severe (average VAS score 4-9); 5. Have a history of migraine for more than one year; 6. Have not received acupuncture treatment within 1 month; 7. Volunteer to participate and sign the informed consent; 8. No other trials were taken within three months.

Exclusion criteria

Exclusion criteria: 1. Patients with bilateral or alternating unilateral migraine; 2. People with a history of head trauma, other primary headaches and headaches of unknown diagnosis, or cervicogenic headache; 3. Combined with serious primary diseases such as cardiovascular and cerebrovascular, liver, kidney and hematopoietic systems and other organic diseases; 4. Combined with severe anxiety, depression, insomnia, and another psychiatric disease or intellectual disabilities who cannot cooperate with the questionnaire, or infection, bleeding disorders, allergies and skin diseases; 5. Pregnancy, lactation, or those who have fertility requirements in the next 6 months. 6. Long-term or current use of analgesic drugs and psychotropic drug dependence. 7. Cannot understand or record the headache diary; 8. Those who have participated in similar research within 3 months.

Design outcomes

Primary

MeasureTime frame
Days of migraine attacks;

Secondary

MeasureTime frame
Frequency of migraine attacks;Intensity of migraine;migraine duration;the dose of intake of acute medication;Migraine Specific Quality of Life Questionnaire, MSQ;Migraine Disability Assessment, MIDAS;Headache impact scale;pittsburgh sleep quality index, PSQI;

Countries

China

Contacts

Public ContactGuo Taipin

Yunnan University of Chinese Medicine

gtphncs@126.com+86 18487272658

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 12, 2026