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Research on the Clinical Effect of Effective Prescription in Treating Unstable Angina.

Research on the Clinical Effect of Effective Prescription in Treating Unstable Angina.

Status
UNKNOWN
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03171597
Enrollment
240
Registered
2017-05-31
Start date
2017-08-31
Completion date
2019-12-31
Last updated
2017-05-31

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

Conditions

Unstable Angina

Keywords

Unstable Angina, Traditional Chinese Medicine

Brief summary

This study evaluates the clinical efficacy of the famous prescription in the treatment of unstable angina pectoris. All of the patients will be divided into 4 arms according to their syndrome type. One of the arms will be treated by conventional western medicine, the other three will be treated by different Chinese herbal medicine prescription at the base of conventional western medicine.

Detailed description

Xuefu Zhuyu Decoction has the function of activating qi and promoting blood circulation, which will be used to treat patients with qi stagnation and blood stasis syndrome. GualouXiebaiBanxia Decoction compounded with Danshen Decoction has the effect of promoting blood circulation and resolving phlegm, so it will be used for patients taht belong to phlegm and blood stasis type. Shuanghe Decoction has the function of supplementing Qi and activating blood circulation, which will be used to treat patients with Qi deficiency and blood stasis syndrome.

Interventions

Including aspirin and clopidogrel, etc.

Mainly including statins

Mainly including nitrates

Mainly including Peach Kernel, Safflower, Angelica, Bupleurum etc.

Mainly including Fructus Trichosanthis, Rhizoma Pinelliae, Allium, Salvia Miltiorrhiza etc.

Mainly including Ginseng, Poria, Calamus, Cyperus, Salvia miltiorrhiza, Radix Polygalae etc.

Sponsors

Jun Li
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
35 Years to 70 Years
Healthy volunteers
No

Inclusion criteria

* Participants diagnosed with coronary heart disease through coronary angiography or coronary CTA; Patients have at least one of these symptoms: 1. The stability of the nature of angina pectoris changes, that is, frequent attacks of angina pectoris, serious degree and prolonged duration; 2. Angina pectoris during rest; 3. The recent occurrence of angina pectoris caused by mild physical activity in the last month.

Exclusion criteria

* Patients dignosed with stable angina; Patients with acute myocardial infarction; Chest pain caused by congenital heart disease, valvular heart disease, severe neurosis or arrhythmia; The heart function grade is III or IV; Patients with acute cerebral infarction; Patients complicated with other serious primary diseases; Patients with acute infection in recent 2 weeks; Uncontrolled hypertension (the resting blood pressure \>160/95mmHg within one week); Diabetics emerged with serious diabetic complications; Patients can't finish the questionnaire due to abnormal mental and nervous or mental disorders; Pregnant or lactating women.

Design outcomes

Primary

MeasureTime frameDescription
MortalitySix months after drug interventionDeath caused by cardiovascular disease

Secondary

MeasureTime frameDescription
Myocardial enzymesAt baseline and 4 weeks after drug interventionThe unit is mmol/L
Blood lipidAt baseline and 4 weeks after drug interventionThe unit is mmol/L.
Treadmill exercise testAt baseline and 4 weeks after drug interventionThe result will be positive or negative
The incidence of myocardial infarction or heart failureSix months after drug intervention

Contacts

Primary ContactPanpan Tian
15652388175@163.com+86 15652388175

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026