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Clinical Study of Qi-Shao-Tong-Mai-An-Shen Decoction (QSTMASD) Regimen for Coronary Heart Disease Syndrome of Qi Deficiency and Blood Stasis Patients with Anxiety and/or Depression

Transformation Research on the Application of Psychological Assessment and Early Warning System in Sino-Japanese Friendship Hospital in the Cooperative Management of Patients with Chinese and Western Medicine

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2200006722
Enrollment
Unknown
Registered
2022-10-31
Start date
2022-11-01
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 heart disease with anxiety and/or depression

Interventions

Treatment group :Standard western medicine treatment for CHD as mentioned above combined with QSTMAS Herbal Paste
Control group:Standard western medicine treatment for CHD

Sponsors

China-Japan Friendship Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: a)Confirmed to the diagnostic criteria of SCAD; b)Confirmed to TCM syndrome of Qi deficiency and blood stasis; c)Confirmed to the diagnostic criteria of mild and moderate anxiety and/or depression using psychological evaluation scales and the early warning system of China-Japan Friendship Hospital; d)Age 18-65 years old; e)Accept and cooperate with the trial scheme f)Volunteer to participate in this study and sign the informed consent forms. People Who meet the above requirements were included in this study.

Exclusion criteria

Exclusion criteria: a)Patients who are receiving anxiolytics, antidepressants or drugs for other mental disorders within one month; b)Combined with severe cardiac insufficiency, such as Killip grade II and above; NYHA grade III and above; c)Combined with other serious diseases, such as severe liver and kidney dysfunction (ALT > 3 × upper limits of normal, SCR > 221 µ mol/L); Severe consumption state or malignant tumor; d)Pregnant or lactating women, or those with pregnancy plans; e)Suspicious or definite allergy to Traditional Chinese Medicine or proprietary Chinese medicine; f)Those who use with similar efficacy to the Traditional Chinese Medicine within 2 weeks; g)Those who are participating in other clinical studies now or within one month. If any of the above conditions are met, it will be excluded.

Design outcomes

Primary

MeasureTime frame
GAD-7 and PHQ-9 scale scores;

Countries

China

Contacts

Public Contactxiaoxiang
zryhyyxx@163.com15810314217

Outcome results

None listed

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