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Improvement of Microvascular Dysfunction by Qingkai Huazhuo Huoxue Method

Improvement of Microvascular Dysfunction by Qingkai Huazhuo Huoxue Method

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1900021954
Enrollment
Unknown
Registered
2019-03-17
Start date
2019-04-01
Completion date
Unknown
Last updated
2019-03-25

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

Conditions

Coronary Microcirculation Disorder

Interventions

Experimental group:Basic treatment+ Shexiangtongxin dropping pill

Sponsors

Xinhua Hospital Affiliated to Shanghai Jiaotong University School of Medicine
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Entry criteria (meet all inclusion criteria): 1. Patients with typical or atypical chest pain; 2. Coronary stenosis within 20%; 3. BMI index> 25; 4. In line with the diagnostic criteria of qi deficiency and blood stasis type: the clinical evidence can be seen in the face of Shaohua, chest pain, fatigue, left hand and small pulse cannot afford to be mentally ill, accompanied by dark or dark tongue and other symptoms of blood stasis.

Exclusion criteria

Exclusion criteria: Meet any of the following: 1. Aged >80 years Or <18 years; 2. Liver insufficiency; 3. Kidney dysfuction; 4. Heart failure (EF<50%); 5. History of cancer; 6. Mentally abnormal patients; 7. Pregnant patients; 8. Patients who took the medicine containing the ingredients of She xiang Tong xin Pills in the past 3 months; 9. Patients who have participated in other clinical trials within the past 3 months, or who are unable to cooperate.

Design outcomes

Primary

MeasureTime frame
Adiponectin;leptin;resistin;

Secondary

MeasureTime frame
Chief complaint;Major adverse cardiac events;

Countries

China

Contacts

Public ContactShu Meng

Department of Cardiology, Xinhua Hospital, School of Medicine, Shanghai Jiaotong University

mengshu@xinhuamed.com.cn+86 13916005250

Outcome results

None listed

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