Analysing the Effects of Xingnaojing for Mild-to-severe Acute Ischemic Stroke (NCT04813445) | Clinical Trial Compass
UnknownNot Applicable
Analysing the Effects of Xingnaojing for Mild-to-severe Acute Ischemic Stroke
China72 participantsStarted 2021-05-28
Plain-language summary
The main purpose of this trial is to analyse the Effects of Xingnaojing for Mild-to-severe Acute Ischemic Stroke by Metabonomics, proteomics and clinical parameters.
Who can participate
Age range35 Years – 80 Years
SexALL
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Inclusion Criteria:
* Diagnosis of Acute ischemic strokeï¼›
* Symptom onset within 24 hoursï¼›
* 35 ≤ Age ≤ 80 years;
* 4 ≤ NIHSS ≤ 25;
* Patient or legally authorized representative has signed informed consent.
Exclusion Criteria:
* Expected length of hospital stay is less than 10 days;
* Planned or already receiving intravenous thrombolysis or endovascular treatment;
* Use of drugs with unknown composition within 1 week before enrollment;
* Patients with acute infectious diseases (e.g. acute pneumonia) or taking related drugs within 1 month before treatment in the group;
* Suspected secondary stroke caused by tumor, brain trauma, or hematological diseases;
* Already dependent in activities of daily living before the present acute stroke (defined as modified Rankin Scale score ≥ 2) ;
* Other conditions that cause cardiogenic embolism (e.g., atrial fibrillation, rheumatic heart disease, valvular heart disease);
* Other conditions that lead to motor dysfunction (e.g., severe osteoarthrosis, rheumatoid arthritis);
* Significant renal or hepatic insufficiency (defined as a serum creatinine concentration, alanine aminotransferase (ALT), or aspartate aminotransferase (AST) value that is twice the upper limit of normal);
* Life expectancy of 3 months or less due to other life-threatening illness (e.g.,advanced cancer)
* Other conditions that render outcomes or follow-up unlikely to be assessed;
* Known to be pregnant or breastfeeding;
* Currently receiving an investigational drug.