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Effect of Aromatic and Warming-up Therapy in Coronary Microvascular Disease: a Multicenter, Randomized, Double-blind, Placebo-controlled Clinical Study.

Effect of Aromatic and Warming-up Therapy in Coronary Microvascular Disease: a Multicenter, Randomized, Double-blind, Placebo-controlled Clinical Study.

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2200005704
Enrollment
Unknown
Registered
2022-03-14
Start date
2022-07-01
Completion date
Unknown
Last updated
2023-02-20

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

Conditions

Coronary Microvascular Disease

Interventions

Test group:Kuanxiong Aerosol
Control group:placebo

Sponsors

Xiyuan Hospital, Chinese Academy of Traditional Chinese medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 75 Years

Inclusion criteria

Inclusion criteria: (1) Meet the CMVD diagnostic criteria; (2) All TCM interventions will be stopped for more than 2 weeks or more; (3) Between 20 and 75, men and women; (4) The subject was informed and voluntarily signed the informed consent form.

Exclusion criteria

Exclusion criteria: (1) Patients who had received revascularization within 1 month before enrollment, or who had required revascularization after this coronary angiography. (2) Suffering from obvious liver and kidney diseases, or alanine aminase (ALT), aspartate amino transferase (AST) 1.5 times above the normal upper limit, creatinine (Cre), blood urea nitrogen (BUN) above the normal upper limit; (3) Suffering from serious heart failure, myocardial heart disease, structural heart disease, difficult to control hypertension and other serious cardiovascular diseases; (4) Patients with serious mental illness, hematopoietic diseases, malignant tumors and other major diseases; (5) Pregnancy or preparation for pregnancy Women, lactating women; (6) Participated in or are attending other clinical researchers in the past three months; (7) A suspicious or clear allergy to the study drug. (8) Other circumstances that the research physician does not consider unsuitable to participate in this trial, including but not limited to: the subjects are unable to follow the study protocol and will bring safety risks to the subjects.

Design outcomes

Primary

MeasureTime frame
Coronary flow reserve;Glycosylated hemoglobin;High sensitivity C-reactive protein;Coronary flow reserve fraction;Endothelial cell specific molecule-1;Serotonin;Ischemia modified albumin;Coronary microvascular resistance index;Triglyceride;Low density lipoprotein;High density lipoprotein;Serum soluble growth stimulating factor-2;Homocysteine;serum soluble CD40 ligand;

Secondary

MeasureTime frame
Self rating Anxiety Scale;Self rating Depression Scale;TCM syndrome score;Seattle angina pectoris scale;

Countries

China

Contacts

Public ContactZhao Fuhai
13911134962@163.com13911134962

Outcome results

None listed

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