Skip to content

Efficacy and safety of salvianolate injection in elderly patients with unstable angina pectoris

Efficacy and safety of salvianolate injection in elderly patients with unstable angina pectoris

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-IPR-17010481
Enrollment
Unknown
Registered
2017-01-19
Start date
2016-05-11
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

unstable angina pectoris

Interventions

treatment group:Experimental drug: salvianolate
control group:ordinary drug

Sponsors

Chinese General Hospital of PLA
Lead Sponsor

Eligibility

Sex/Gender
All
Age
60 Years to 85 Years

Inclusion criteria

Inclusion criteria: 1. Patient in line with 1979 WHO diagnostic criteria for UA; 2. Aged 60-85 years; 3. Traditional Chinese medicine for CHD treatment should be stopped at least 1 week;take CHD drugs standardly; 4. Participates give written informed consent.

Exclusion criteria

Exclusion criteria: 1. NSTE-ACS caused by non atherosclerotic disease; 2. Angina pectoris caused by violent activities, fever, tachycardia, high adrenergic state, mental stress, lack of sleep, eating too full, left ventricular load increased (hypertension, aortic stenosis); 3. Angina pectoris caused byanemia, methemoglobinemia and hypoxemia; 4. Abnormal thyroid function; 5. Poorly controlled hypertension (systolic pressure =160mmHg or diastolic blood pressure =100mmHg); 6. Severe cardiopulmonary dysfunction; 7. Severe arrhythmia (atrial fibrillation, atrial flutter, paroxysmal ventricular tachycardia, sinus bradycardia (heart rate < 55), complete left bundle branch block; 8. Combined liver and kidney and hematopoietic system and other serious diseases, liver function (ALT, AST) 3 times higher than the upper limit of normal renal function, creatinine clearance rate (CrCl) less than 30 ml/min/1.73m2; 9. Recent 4 weeks underwent surgery and bleeding tendency; 10. Poor compliance; 11. At the same time in other clinical researches; 12. Allergic constitution.

Design outcomes

Primary

MeasureTime frame
symptom of angina pectoris;

Secondary

MeasureTime frame
Seattle angina scale score;EQ-5D health scale;TIMI risk score;Incidence of cardiovascular and cerebrovascular events;

Countries

China

Contacts

Public ContactLi Xiaoying

General Hospital of PLA

xyli301@163.com+86 13501230797

Outcome results

None listed

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