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Transcriptomics and Metabolomics Research on Acute Cerebral Infarction (Blood Stasis Syndrome)

Transcriptomics and Metabolomics Research on Acute Cerebral Infarction (Blood Stasis Syndrome)

Status
Recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2100046072
Enrollment
Unknown
Registered
2021-05-03
Start date
2021-05-01
Completion date
Unknown
Last updated
2021-12-13

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

Conditions

Acute Cerebral Infarction

Interventions

Sponsors

The Affiliated Hospital of Changchun University of Traditional Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: [Inclusion criteria for patients with cerebral infarction] 1. Meet the diagnostic criteria of western medicine for acute cerebral infarction; 2. Comply with the diagnostic criteria of the Chinese meridian (blood stasis syndrome) in the acute phase of ischemic stroke in traditional Chinese medicine; 3. The onset time is less than 14 days; 4. 3 <= NIHSS < 15 points; 5. Aged 45 to 65 years; 6. The patient voluntarily signed an informed consent form. [Inclusion criteria for healthy volunteers] 1. Sign the informed consent form before the test, and have a full understanding of the test content, process and possible risks; Able to complete the research in accordance with the requirements of the test plan; 2. Male and female subjects aged 45 to 65 years (including 45 and 65 years old); 3. The weight of male subjects is not less than 50kg, and the weight of female subjects is not less than 45kg. Body mass index (BMI) = weight (kg)/height 2 (m2), the body mass index is within the range of 18-28kg/m2 (including the critical value); 4. Health status: clinically significant medical history such as heartlessness, liver, kidney, digestive tract, nervous system, respiratory system, mental abnormalities and metabolic abnormalities; 5. Physical examination and normal or abnormal vital signs have no clinical significance.

Exclusion criteria

Exclusion criteria: [Exclusion criteria for patients with cerebral infarction] 1. A comatose patient; 2. Those who need or have undergone thrombolysis or endovascular treatment; 3. Patients with allergies; 4. Patients whose blood pressure is still less than 90/60mmHg or >= 220mmHg/120mmHg after treatment; 5. Complicated with severe liver and kidney damage, and whose ALT, AST, Cr, and BUN levels are 1.5 times higher than normal; 6. Accompanied by other complications and complications that affect drug evaluation, such as severe cardiac insufficiency, severe mental illness, depression and dementia after stroke, cerebral hemorrhage after cerebral infarction, etc.; 7. Has had a stroke in the past; 8. Disabled patients (blindness, deafness, dumbness, intellectual disability, mental disability, etc.) stipulated by law, and physical disability caused by other diseases affect the assessors of neurological impairment; 9. Those with bleeding tendency or severe bleeding within 3 months; 10. Suspected or true history of alcohol or drug abuse, or other circumstances that reduce the possibility of enrollment or complicate enrollment based on the judgment of the investigator; 11. Menstrual period women, pregnant women and lactating women, those who have a positive pregnancy test or have recent birth plans; 12. Participating in other clinical trials or participating in other drug clinical trials within 3 months. [Exclusion criteria for healthy volunteers] 1. Donate blood or lose a lot of blood (>450mL) within three months before screening; 2. There have been major changes in diet or exercise habits recently; 3. Female subjects are breastfeeding during the screening period or during the test, or the result of serum pregnancy is positive; 4. Those who have a history of drug abuse or have used drugs in the past five years; 5. Other factors lead the researcher to believe that he cannot enter the experiment.

Design outcomes

Primary

MeasureTime frame
Transcriptomics differential genes;Metabolomics differential metabolites;

Countries

China

Contacts

Public ContactZhao Dexi

Changchun University of Chinese Medicine

dezizhao1006@163.com+86 15948000773

Outcome results

None listed

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