Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-25 @ 2:36 AM
Ignite Modification Date:
2025-12-25 @ 2:36 AM
NCT ID:
NCT03091634
Eligibility Criteria:
Inclusion Criteria:
* The participants diagnosed as QS\&BSS;
* The age of participants is from 18 to 65;
* Participants who voluntarily signed informed consent.
Exclusion Criteria:
* Participants with other obvious Chinese medicine syndrome
* Participants diagnosed as acute myocardiac infarction, acute phase of cerebral infarction, aortic dissection and other critically illness;
* Participants with poor control of hypertension (systolic pressure \>160 millimeters of mercury (mmHg) or diastolic blood pressure \>100mmHg), severe heart failure and severe arrhythmia (atrial fibrillation, atrial flutter, ventricular tachycardia, paroxysmal II type II atrioventricular block and complete bundle branch block);
* Participants with severe primary diseases of heart, brain, liver, kidney and hematopoietic system, or liver function ALT or AST value \>1.5 times of the upper limit of the normal value, or abnormal renal function;
* Depression or anxiety disorders participants;
* Pregnant or lactating women;
* Participants with nerve or mental illness, or unwilling to cooperate participants;
* Participants have performed a surgery in the past 4 weeks;
* Participants with the tendency of bleeding or abnormal value of disseminated intravascular coagulation (DIC) or International standard ratio (INR) or thrombocytopenia patients;
* Participants have joined in other trial in the past 1 month;
* Participants allergic to the test drug, or people with allergic constitution;
* Participants with aphasia which affects data collection.
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Maximum Age:
65 Years
Study:
NCT03091634
Study Brief:
Protocol Section:
NCT03091634