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Clinical efficacy and mechanism of Qingqiao Congming Decoction in the treatment of migraine

Clinical efficacy and mechanism of Qingqiao Congming Decoction in the treatment of migraine

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2025001908
Enrollment
Unknown
Registered
2025-10-15
Start date
2025-09-01
Completion date
Unknown
Last updated
2025-11-17

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

Conditions

migraine

Interventions

treatment group:Qingqiao Congming Decoction
control group:placebo

Sponsors

Gansu Provincial Hospital of Traditional Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1) Age range: 18 - 65 years old, gender not restricted; 2) Meets the diagnostic criteria for migraine as defined in the "International Classification of Headache Disorders Version 3" (ICHD-3) (including either a migraine without aura or with aura); average weekly headache duration (converted) is = 1 day and = 4 days. 3) Voluntarily participates in this study, signs the informed consent form, has good compliance, and can be followed up on time; 4) Has not received any other systemic preventive treatment for migraine in the past 1 month.

Exclusion criteria

Exclusion criteria: 1) Pregnant women, lactating women or those with a pregnancy plan within the past six months; 2) Those with secondary headaches (such as tumors, brain trauma, infections, etc.); 3) Patients who have used migraine prevention drugs (such as CGRP monoclonal antibodies) within the past month; 4) With abnormal laboratory indicators (ALT/AST > 1.5 times the upper limit, eGFR < 60 ml/min); 5) Patients with organic lesions in important organs such as the heart, lungs, liver, and kidneys, or those with mental disorders and other reasons that prevent them from cooperating with the trial; 6) Those allergic to the test drugs and their excipients; 7) Those undergoing other treatments or participating in other clinical research studies; 8) Those judged by the researchers to be unsuitable for inclusion in this trial.

Design outcomes

Primary

MeasureTime frame
Frequency of migraine attacks (average per week) changes;Duration of migraine (hours) variation;

Secondary

MeasureTime frame
Change in headache intensity (VAS score);Traditional Chinese medicine syndrome scoring (including the nature of headache, tongue appearance, pulse characteristics, etc.);Migraine Impact Scale (MSQ);HIT-6 score;Migraine Disability Assessment;Anxiety/Depression Assessment;

Countries

China

Contacts

Public ContactZhang Zhiming

Gansu Provincial Hospital of Traditional Chinese Medicine

zhangzhimingys@163.com13099267516

Outcome results

None listed

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