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Clinical Trials/ITMCTR1900002466
ITMCTR1900002466
Not yet recruiting
Phase 1

Study for the prevention and treatment of hypertensive cerebral small vessel disease by Naotaifang

Hu'nan University of Chinese Medicine0 sitesTBD

Overview

Phase
Phase 1
Intervention
Not specified
Conditions
Not specified
Sponsor
Hu'nan University of Chinese Medicine
Status
Not yet recruiting
Last Updated
3 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
3 years ago
Study Type
Interventional study
Sex
All

Investigators

Sponsor
Hu'nan University of Chinese Medicine

Eligibility Criteria

Inclusion Criteria

  • 1\. Agec between 40\-80 years old;
  • 2\. Compliance with patients with essential hypertension;
  • 3\. According to the General Consensus of Diagnosis and Treatment of Cerebral Small Vascular Diseases, MRI confirmed cerebral small vessel disease, but yes or no clinical manifestations of brain damage;
  • 4\. TCM syndrome differentiation standard: refer to the Interpretation of TCM Clinical Diagnosis and Treatment Guidelines. Syndrome based on wind\-phlegm stagnant blood syndrome;
  • 5\. Voluntary participation in the trial and signing of informed consent.

Exclusion Criteria

  • 1\. Serious life\-threatening diseases such as acute myocardial infarction, stroke, cardiac insufficiency, grade IV, etc;
  • 2\. Imaging and other diseases to exclude hypertensive cerebral small vessel disease;
  • 3\. Hypertension can not be controlled by using antihypertensive drugs;
  • 4\. Patients with cerebral macrovascular disease;
  • 5\. Allergic or research drug known to be allergic to ingredients;
  • 6\. Suspected or indeed have a history of alcohol or drug abuse, or according to the judgment of the investigator, other lesions or conditions that reduce the likelihood of enrollment or complicate the enrollment, such as frequent changes in the working environment and unstable living environment, may cause loss of follow\-up Case;
  • 7\. Suffering from any serious psychological abnormalities and mental disorders, unable to comply with clinical research procedures and norms, and other researchers believe that it is not suitable for inclusion;
  • 8\. Preparing a pregnant or lactating woman within one or six months of pregnancy;
  • 9\. Patients who are participating in other clinical trials or have participated in other clinical trials in the past month.

Outcomes

Primary Outcomes

Not specified

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