內容目錄
This local star homemade potion
Looking forward to your help!
The Department of Encephalopathy of Enshi Central Hospital will carry out a “Clinical Trial Study on Evaluating the Efficacy and Safety of Toutongning Capsules in Treating Migraine (Blood Stasis Syndrome) Patients”, which is now open to the public. Recruit patients, and all patients who meet the requirements through pre-enrollment screening will have the opportunity to participate in the clinical study.
【Research Background】
Toutongning Capsule is a traditional Chinese medicine preparation approved by the Provincial Food and Drug Administration and independently developed by Enshi Central Hospital. It has been used in the hospital for more than 20 years and is widely praised by patients. . At present, with the strong support of the Provincial Health Commission and the Provincial Food and Drug Administration, the hospital has signed a strategic cooperation agreement with Grand Pharmaceutical (China) Co., Ltd., which will make full use of the professional advantages and resources of both sides of the hospital and enterprises to carry out research and development in the field of drugs. All-round cooperation to promote pharmaceutical preparations and cutting-edge innovative research, achievement transformation and development and marketing. Toutongning Capsules, as a “star homemade medicine”, will be developed and marketed in advance.
In order to more objectively understand the efficacy of Toutongning Capsules in the treatment of migraine, so that more migraine patients have the opportunity to control and improve their condition, the headache expert team of Enshi Central Hospital’s Department of Encephalopathy launched this research project.
1. Research purpose
To evaluate the efficacy and safety of Toutongning Capsules in the treatment of migraine (blood stasis syndrome) patients.
2. Eligibility criteria
(1) Age between 18 and 60 years old, age of first migraine attack ≤ 50 years old;
(2) Traditional Chinese Medicine Diagnosed as headache disease, and the syndrome differentiation is blood stasis block syndrome;
(3) The duration of migraine is ≥1 year, the number of attacks is ≥2 times per month in the past 3 months, and the number of headache days per month is 15 days or more. The following;
(4) The patient himself signed the informed consent voluntarily.
(For the full version of the inclusion criteria, see the study protocol.)
3. Recruitment time
From now until December 31, 2022
IV. The benefits of participating in the study
The patients and society may benefit from this study include:
1. The patient’s headache symptoms may be improved, and this item The research may support the marketing of a new traditional Chinese medicine for migraine for use in other patients with similar conditions;
2. Patients will receive good medical care during the study.
V. Research-related expenses and subsidies
Provide patients with free examination and treatment drugs related to this clinical trial; patients participating in this research will receive a certain amount of transportation subsidies .
If you are willing to participate in the research and believe that you meet all the requirements of the research, you can contact us:
Contact:
Huang Nianping (13872720234)
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Huang Xinquan (13971895543)
Li Xuejie (13872735758)
Address:
No.178 Hangkong Avenue, Enshi City
Enshi The outpatient department of encephalopathy on the second floor of the comprehensive building of the Department of Traditional Chinese Medicine of the State Central Hospital (Enshi State Hospital for Nationalities).
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