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Observing the effect of Tongnao Yin on the stability of carotid plaque based on OCT technology

Observing the effect of Tongnao Yin on the stability of carotid plaque based on OCT technology

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100044893
Enrollment
Unknown
Registered
2021-03-31
Start date
2021-04-01
Completion date
Unknown
Last updated
2021-11-02

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

Conditions

Carotid atherosclerosis

Interventions

Treatment group :Tongnaoyin with basic therapy and atorvastatin
Control group :basic therapy and atorvastatin

Sponsors

Jiangsu Provincial Hospital of Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1.Aged 40 to 75 years; 2.No patients with cerebral hemorrhage or brain tumor were found by CT or MRI of the head; 3.Patients showed vulnerable plaque through carotid artery ultrasound and carotid artery contrast-enhanced ultrasound examination, or suspected to be vulnerable plaque requiring OCT. 4.Accept DSA examination and meet OCT carotid atherosclerosis vulnerable plaque; 5.Carotid artery lumen stenosis between 50%-70%; 6.Combined with the tongue veins,TCM syndrome differentiation belongs to Phlegm and Blood Stasis Syndrome; 7.Patients who have good compliance, agree to participate in the trial, and sign an informed consent form;

Exclusion criteria

Exclusion criteria: 1.There are clear contraindications to the use of antiplatelet drugs; 2.Allergies, such as those with a history of allergies to two or more drugs or foods, those who have been allergic to statins, Chinese patent medicines containing leeches, or suspected of allergies to leeches; 3.Abnormal liver and kidney function or severely elevated muscle enzymes (ALT, AST> 1.5 times the upper limit of normal, Cr> upper limit of normal); 4.Patients with severe gastrointestinal diseases such as stomach and duodenal ulcers and perforation, which affect the absorption of drugs; 5.Have serious primary heart, liver, lung, kidney, blood or serious diseases that affect their survival, such as tumor or AIDS; 6.Patients with a history of mental illness or disability; 7.Other lesions that, in the investigator's judgment, reduce the likelihood of inclusion or complicate inclusion, such as frequent changes in the work environment, may lead to loss of follow-up; 8.Patients who are participating in clinical observation of other drugs.

Design outcomes

Primary

MeasureTime frame
Stability of plaque;

Secondary

MeasureTime frame
Traditional Chinese Medicine (TCM) syndrome efficacy;Acute event rate of ischemic cerebrovascular disease;

Countries

China

Contacts

Public ContactWu Minghua

Jiangsu Provincial Hospital of Chinese Medicine

mhuawu@163.com+86 13951786719

Outcome results

None listed

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