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Study for the clinical evaluation of Yi-Qi-Tong-Luo granule in the treatment of qi deficiency and blood stasis

Study for the clinical evaluation of Yi-Qi-Tong-Luo granule in the treatment of qi deficiency and blood stasis

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1800019585
Enrollment
Unknown
Registered
2018-11-19
Start date
2018-05-01
Completion date
Unknown
Last updated
2018-11-26

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

Conditions

Qi deficiency and blood stasis syndrome(Convalescence of ischemic stroke?stable coronary artery disease?diabetic peripheral neuropathy)

Interventions

Group 2:Conventional treatment + Yi-Qi-Tong-Luo granule
Group 1:Conventional treatment + Yi-Qi-Tong-Luo granule placebo

Sponsors

Ethics Committee of Dongzhimen Hospital Affiliated to Beijing University of Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
35 Years to 80 Years

Inclusion criteria

Inclusion criteria: Convalescence of ischemic stroke: (1) diagnosis of qi deficiency and blood stasis; (2) consistent with the western medical diagnosis of ischemic stroke; (3) aged between 35 and 80 years; (4) the onset is within 2 weeks to 3 months; (5) NIHSS score 4-22; (6) sign the informed consent. stable coronary artery disease: (1) diagnosis of qi deficiency and blood stasis syndrome; (2) in line with the western medicine stability of coronary heart disease angina pectoris I-III level diagnosis; (3) aged between 35 and 80 years; (4) signing the informed consent. Diabetic peripheral neuropathy: (1) diagnosed as qi deficiency and blood stasis; (2) meet the western diagnostic criteria for diabetic peripheral neuropathy; (3) between the ages of 35 and 80 years; (4) signing the informed consent.

Exclusion criteria

Exclusion criteria: Convalescence of ischemic stroke: (1) patients with stroke caused by brain tumors, brain trauma, and blood diseases; (2) patients with other diseases that affect the function of the limbs and affect the neurologic examination; (3) patients with severe hepatic and renal insufficiency (note: liver insufficiency refers to the value of ALT or AST greater than 2 times the normal upper limit;Renal insufficiency refers to blood creatinine value greater than 2 normal upper limit); (4) other diseases or psychoses that may affect patients' follow-up; (5) women who are pregnant or preparing for pregnancy or lactation; (6) those who are known to be allergic or severely allergic to the drug ingredients; (7) a witness with red tongue and thick tongue coating; (8) are participating in clinical trials of other drugs. Stable coronary artery disease: (1) patients with acute myocardial infarction, coronary heart disease in 3 month IV level/severe angina pectoris and other heart disease, other causes of chest pain; (2) patients with severe cardiopulmonary insufficiency, severe arrhythmia (rapid atrial fibrillation, atrial flutter, paroxysmal ventricular tachycardia, etc.); (3) patients with severe hepatic and renal insufficiency; (4) other diseases or psychoses that may affect patients' follow-up; (5) women who are pregnant or preparing for pregnancy or lactation; (6) those who are known to be allergic or severely allergic to the drug ingredients; (7) a witness with red tongue and thick tongue coating; (8) are participating in clinical trials of other drugs. Diabetic peripheral neuropathy: (1) acute and severe diabetes; (2) accompanied by severe heart and brain diseases; (3) patients with severe hepatic and renal insufficiency (note: liver insufficiency refers to the value of ALT or AST greater than 2 times the normal upper limit; (4) Severe renal insufficiency refers to patients with spinal cord injury, cervical and lumbar pushing (nerve root compression, spinal canal stenosis, cervical and lumbar degeneration) or cerebrovascular diseases sequelae, neuromuscular joint or muscle diseases; (5) neuropathy caused by other diseases; (6) other diseases or psychoses that may affect patients' follow-up; (7) women who are pregnant or ready for pregnancy or lactation; (8) those who are known to be allergic to or severely allergic to the drug ingredients; (9) a witness with red tongue and thick tongue coating; (10) are participating in clinical trials of other drugs.

Design outcomes

Primary

MeasureTime frame
Evaluation scale of qi deficiency and blood stasis syndrome;

Countries

China

Contacts

Public ContactGao Ying

Dongzhimen Hospital Affiliated to Beijing University of Chinese Medicine

gaoying973@126.com+86 13366275973

Outcome results

None listed

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