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The Effect of Erigeron Injection on Acute Cerebral Infarction Serum VEGF, MMP-9 and EPC Levels

The Effect of Erigeron Injection on Acute Cerebral Infarction Serum VEGF, MMP-9 and EPC Levels

Status
UNKNOWN
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01926834
Enrollment
60
Registered
2013-08-21
Start date
2013-08-31
Completion date
2014-03-31
Last updated
2013-08-21

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

Conditions

Cerebral Infarction

Keywords

promoting angiogenesis in multiple targets, herbal medicine, traditional chinese medicine, random clinical trial

Brief summary

To study the effects of Erigeron Injection on human serum VEGF, MMP-9 and EPC levels after acute cerebral infarction,test is made by random double-blind controlled.patients with acute cerebral infarction were divided randomly into erigeron injection+aspirin group,aspirin group,and health people. The main indexes are the serum level of VEGF, MMP-9 and EPC.The review is made by the reference to NIHSS and so on. So, Erigeron Injection have the function of promoting angiogenesis in multiple targets through this test.

Detailed description

OBJECTIVE: To study the effects of Erigeron Injection on human serum VEGF, MMP-9 and EPC levels after acute cerebral infarction. METHOD: 40 patients with acute cerebral infarction(in accordance with the inclusion criteria) were divided randomly into erigeron injection+aspirin group,aspirin group,and 20 health people. Erigeron injection+aspirin group and aspirin group drew peripheral blood on the prior treatment,the posttreatment 1th, 3th and 7th day,and tested the level of VEGF, MMP-9 and EPC.Tested the health people one time.

Interventions

DRUGErigeron Injection

Erigeron Injection, 30ml, iv, qd, for 7days

DRUGplacebo

normal saline, 500ml,i.v.,qd, for 7 days

Sponsors

Guangzhou University of Traditional Chinese Medicine
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* patients aged no younger than 18yrs * attack within 72 hours * NIHSS score in the 2-25 points * Ischemic Stroke occurred for the first time, or with a history of stroke disease but without sequelae * Signed the informed consents

Exclusion criteria

* patients aged younger than 18yrs * Patients with tumor, coronary heart disease, valvular heart disease, psoriasis, rheumatism, hematologic diseases, infertility, varieties of acute inflammation * Patients with severe cognitive impairment * Refused to cooperate or been unable to cooperation for neurological disorders * Cerebral hemorrhage or hemorrhagic cerebral infarction * Unstable vital signs dued to massive cerebral infarction * Patients with serious heart, liver and renal insufficiency

Design outcomes

Primary

MeasureTime frame
the serum level of VEGF,MMP-9 and EPC0-7days

Secondary

MeasureTime frame
National Institute of Health of stroke scale0-7days

Contacts

Primary ContactJianwen Guo, doctor
jianwen_guo@msn.com0086-13724899379
Backup ContactYefeng Cai, master
caiyefeng@126.com(08620)81887233

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026