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A randomized controlled study on the analgesic treatment of migraine in acute phase with the combination of horizontal penetration needling and rizatritan

A randomized controlled study on the analgesic treatment of migraine in acute phase with the combination of horizontal penetration needling and rizatritan

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2024000156
Enrollment
Unknown
Registered
2024-08-01
Start date
2024-08-15
Completion date
Unknown
Last updated
2024-08-19

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

Conditions

migraine

Interventions

Acupuncture combined with medicine group:horizontal penetration needling and rizatriptan monobenzoate tablets
Western medicine group:rizatriptan monobenzoate tablets
Acupuncture group:horizontal penetration needling

Sponsors

Nanjing Hospital of Traditional Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 50 Years

Inclusion criteria

Inclusion criteria: 1) Meet the diagnostic criteria of migraine without aura and migraine with aura; 2) Aged 18-50 years, with a history of migraine for more than 12 months; 3) In the acute phase, the pain degree was evaluated by visual analogue scale (VAS) method with 4 points or more; 4) Patients voluntarily received relevant acute analgesia treatment and signed informed consent.

Exclusion criteria

Exclusion criteria: 1) Patients with hypertension and current unstable blood pressure control (stage 2, high-risk patients and above), coronary heart disease (including patients with pacemakers), cerebral infarction and other cardiovascular and cerebrovascular stenosis or obstructive diseases, peripheral vascular stenosis and obstruction; 2) Patients with severe primary diseases such as liver, kidney, digestion and blood system; 3) Mental patients, or patients with infection and bleeding; 4) Pregnant or lactating women; 5) Patients with organic lesions; 6) Patients who cannot understand and cooperate with the visual analogue scale (VAS) method.

Design outcomes

Primary

MeasureTime frame
2h Headache remission rate;

Secondary

MeasureTime frame
2h headache disappearance rate;24h headache remission rate;24h headache disappearance rate;

Countries

china

Contacts

Public ContactRenzhong Kou

Nanjing Hospital of Traditional Chinese Medicine

530950775@qq.com15861813731

Outcome results

None listed

Source: ITMCTR (via WHO ICTRP) · Data processed: Feb 4, 2026