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Proteomic Study of Chuanhong Zhongfeng Capsule in the Treatment of ACI

Y

Yingyue Ding

Status and phase

Completed
Phase 1

Conditions

Acute Ischemic Stroke

Treatments

Drug: Chuanhong Zhongfeng capsule

Study type

Interventional

Funder types

Other

Identifiers

NCT06874140
CCZYFYKYLL2023
2022JC046 (Other Grant/Funding Number)

Details and patient eligibility

About

Acute cerebral infarction is characterized by high disability rate and high recurrence rate, which poses a great threat to the life and health of the nation. Proteomics technology is a holistic and comprehensive understanding of disease mechanism, cell metabolism and other processes at the protein level. The correlation between acute cerebral infarction and proteomics has become a hot spot of clinical and basic research in recent years. Chuanhong Zhongfeng capsule was developed by Ren Jixue, a master of national medicine, and clinical studies have confirmed that it not only promotes the recovery of neurological function in patients with cerebral infarction, reduces the disability rate, but also improves the long-term prognosis, but its mechanism of action and its target are still unclear. In the present study, we applied 4D Label-free proteomics technology and PRM technology to study for the first time the mechanism of action and potential targets of Chuanhong Zhongfeng Capsule in the treatment of acute cerebral infarction, which will provide a direction for the study of traditional Chinese medicine compounding for the prevention and treatment of cerebral infarction.

Enrollment

20 patients

Sex

All

Ages

40 to 80 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. Meet the diagnostic criteria for ischemic stroke in the Chinese Guidelines for Diagnosis and Treatment of Ischemic Stroke in the Acute Phase 2018.
  2. Meet the diagnostic criteria for ischemic stroke in Chinese medicine.
  3. Within 2 weeks of acute onset of ischemic stroke.
  4. 4 ≤ NIHSS score <15.
  5. Age 40-80 years old. -

Exclusion criteria

  1. Diagnosis of hemorrhage or other pathological brain disorders based on head CT or MRI;
  2. Allergic individuals, those who are allergic to the test medication or the associated medicinal flavors or components thereof;
  3. Age <40 years or >80 years;
  4. Those with severe liver or kidney function impairment. -

Trial design

Primary purpose

Other

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

20 participants in 2 patient groups

Chuanhong Zhongfeng capsule
Experimental group
Description:
Basic treatment (refer to China Acute Ischemic Stroke Diagnosis and Treatment Guidelines 2018) + Chuanhong Zhongfeng capsule
Treatment:
Drug: Chuanhong Zhongfeng capsule
control
Active Comparator group
Description:
Basic treatment (refer to Chinese Guidelines for the Diagnosis and Treatment of Acute Ischemic Stroke 2018)
Treatment:
Drug: Chuanhong Zhongfeng capsule

Trial documents
2

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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