Overview

Multi-"Omics" Research of Danhong Injection to Treat Acute Ischemic Stroke

Status:
Completed
Trial end date:
2020-07-01
Target enrollment:
0
Participant gender:
All
Summary
The purpose of this study is to explore the pharmacological mechanism of Danhong injection in the treatment of acute ischemic stroke.
Phase:
Phase 4
Accepts Healthy Volunteers?
Accepts Healthy Volunteers
Details
Lead Sponsor:
China Academy of Chinese Medical Sciences
Collaborator:
China Food and Drug Administration
Criteria
Inclusion Criteria:

1. Female or male inpatients

- Age: 18 - 70 years.

- Clinical diagnosis of ischemic stroke causing a measurable neurological deficit
defined as impairment of language, motor function, cognition and/or gaze, vision
or neglect. Ischemic stroke is defined as an event characterized by the sudden
onset of an acute focal neurologic deficit presumed to be due to cerebral
ischemia after CT scan excludes hemorrhage.

- Clinical diagnosis of "Xueyu Zheng" (Blood Stasis Syndrome) as the scores of
Chinese medicine symptoms scales of "Xueyu Zheng" in ischemic stroke ≥ 20. The
Chinese medicine symptoms scales of "Xueyu Zheng" is defined as following
(1)hemiplegia-10,(2)numbness of limbs-10,(3) dark face-9,(4)purple or dark
lip-8,(5)Roughness of skin-4, (6) pain with fixed point-5, (7) purple or dark
tongue-10,(8)ecchymosis on tongue-10,(9)purple sublingual vessel-10,(10)varicose
sublingual vessel-8,(11)unsmooth pulse-8,(12)intermittent pulse-1.

- Onset of symptoms in 1 week prior to initiation of administration of study drug.

- Clinical diagnosis of cerebral anterior circulation obstruction.

- 4≤NIHSS<20.

- Patient is willing to participate voluntarily and to sign a written patient
informed consent. Informed consent will be obtained from each patient or the
subject's legally authorized representative or relatives, or deferred where
applicable, according to the regulatory and legal requirements of the
participating centers.

2. Female or male healthy volunteer

- Age: 18 - 70 years.

- Medical history, physical examination, vital signs, electrocardiogram(ECG) and
laboratory results (including renal function, hepatic function, et al)with no
clinically significant findings.

- Healthy volunteer is willing to participate voluntarily and to sign a written
informed consent form. Informed consent will be obtained from each volunteer,
according to the regulatory and legal requirements of the participating centers.

Exclusion Criteria:

1. Female or male inpatients

- Evidence of intracranial hemorrhage (ICH) or other cerebral diseases (eg.vascular
malformation, tumor, abscess or multiple sclerosis etc.)on the CT-or MRI-scan.

- Patients with thrombolysis or endovascular treatment.

- Known history of allergy or suspected allergic to the drug.

- Blood glucose 2.8 or > 16.8 mmol / l under the treatment of diabetes or with
severe complications due to diabetes (eg. peripheral neuropathy, diabetic
gangrene).

- Liver function impairment with the value of ALT or AST over 1.5-fold of normal
value.

- Renal dysfunction with the value of serum creatinine over 1.5-fold of normal
value.

- Severe cardiac dysfunction on echocardiogram or the grade of heart function over
Ⅲ grade.

- History of prior stroke with mRS ≥2.

- Complicated with atrial fibrillation.

- Severe stroke as assessed by appropriate imaging techniques (eg. massive cerebral
infarction including more than one lobe of brain or over 1/3 of blood-supply area
of middle cerebral artery).

- Prior disable patients.

- Hemorrhagic tendency or recent severe or dangerous bleeding in 3 months.

- Suspected addicted into alcohol or drug abuse.

- With severe complications that would make the condition more complicated assessed
by the investigator.

- Woman with pregnancy, lactation or positive result of pregnancy test, or women
who want to be pregnant in recent 6 months.

- Woman who is under menstrual period.

- Patient who is participating in other trials or has been participated in other
trials in recent 3 months.

2. Healthy volunteer

- Had a known history of chronic diseases including stroke, heart diseases,
diabetes, COPD, Neuropsychiatric diseases and chronic infectious diseases, etc.

- Coagulation disorders.

- Conditions with increased bleeding risk.

- Trauma or surgery in the 6 months prior to the study.

- Use of any medication 4 weeks prior to the trial.

- History of drug abuse.