An Open Label Clinical Trial to Evaluate the Efficacy and Safety of Calculus Bovis Sativus (CBS) for Ischemic Cerebral Vascular Disease

Status: Recruiting
Location: See all (2) locations...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

The most common cause of death for Chinese patients is ischemic cerebrovascular diseases(ICVD), particularly cerebral infarction. It places a heavy burden on people, families, and society as a whole and poses considerable risks of death and disability. The disease known as CSVD has a subtle beginning, is difficult to identify, and is frequently detected only after it progresses to the point of vascular cognitive dysfunction. The primary ischemia necrosis of brain nerve cells and the activation of inflammatory cells are their pathologic processes. According to historical Chinese medical documents, bezoar possesses properties that can help prevent seizures, treat strokes, enhance cognitive function and mental well-being, and stimulate alertness. Calculus Bovis Sativus (CBS) is the most authentic formulation of bezoar ingredients compared to other bezoar products. It has received approval from the China Food and Drug Administration for the essential treatment of comatose patients. CBS consists of three primary constituents: bilirubin, bile acids, and taurine. Scientific evidence has demonstrated that all of these components possess anti-inflammatory, antioxidant, and neuroprotective properties. The investigators' objective is to carry out an investigator-initiated clinical study to assess the efficacy of orally administered CBS in treating ischemic cerebrovascular diseases in humans.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: t
View:

• ICVD cohort:

‣ Subjects are able to understand the purpose and risks of the study, provide informed consent, and authorize the use of confidential health information in accordance with national and local privacy regulations.

⁃ Both men and women are welcome, and the age at the time of providing informed consent is 18-80 years (inclusive).

⁃ All women of childbearing age and all men must use contraceptive measures during the study and for at least 30 days after the last dose of study treatment. In addition, subjects should not donate sperm or eggs during the study and for at least 30 days after the last dose of study treatment.

⁃ Must be diagnosed with

‣ ① Ischemic stroke, according to the Diagnosis Points of Various Cerebrovascular Diseases of the Fourth National Cerebrovascular Disease Academic Conference, the main clinical diagnosis is ischemic stroke (cerebral infarction), 1 point ≤ NIHSS ≤ 24 points, and mRS ≤ 3 points; or ② Cerebral small vessel disease, according to the results of conventional sequence MRI examination, Fazekas score on T2 FLAIR sequence ≥ 3 points (0-6 points, the sum of paraventricular WMH score + subcortical WMH score), and mRS ≤ 3 points (mRS ≤ 4 points for those with recent subcortical small infarction within 1 month).

⁃ Neurological examination showed stability within 30 days before baseline (visit 1).

• Healthy cohort:

‣ Age ≥ 18 years old when signing the informed consent form

⁃ Healthy adult subjects without underlying diseases

Locations
Other Locations
China
Tongji Hospital affiliated to Tongji Medical College of Huazhong University of Science and Technology
RECRUITING
Wuhan
Tongji Hospital of Tongji Medical College, Huazhong University of Science and Technology
RECRUITING
Wuhan
Contact Information
Primary
Ke Shang, MD
kay_sang@qq.com
86-27-83663337
Backup
Ke Shang, MD
kay_sang@hust.edu.cn
86-27-83663332
Time Frame
Start Date: 2024-08-08
Estimated Completion Date: 2029-12
Participants
Target number of participants: 230
Treatments
Experimental: CBS therapy, CBS dosage: 100mg per day from day 1 to day 84, in ICVD cohort
Subjects in ICVD cohort of this arm will receive general therapy plus CBS.
No_intervention: Control therapy: no intervention, in ICVD cohort.
Subjects in ICVD cohort of this arm will only receive general therapy.
Experimental: CBS therapy, CBS dosage: 100mg per day from day 1 to day 84, in healthy cohort
Subjects in healthy cohort of this arm will only receive CBS.
Related Therapeutic Areas
Sponsors
Leads: Tongji Hospital
Collaborators: Jianmin Pharmaceutical Group Co., LTD.

This content was sourced from clinicaltrials.gov