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Efficacy evaluation of dynamic single photon emission computed tomography (D-SPECT) combined with myocardial contrast echocardiography (MCE) in the intervention of Tongxinluo capsule in non-coronary obstructive ischemic heart disease (INOCA)

Efficacy evaluation of dynamic single photon emission computed tomography (D-SPECT) combined with myocardial contrast echocardiography (MCE) in the intervention of Tongxinluo capsule in non-coronary obstructive ischemic heart disease (INOCA)

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100052622
Enrollment
Unknown
Registered
2021-11-02
Start date
2022-01-01
Completion date
Unknown
Last updated
2023-04-12

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

Conditions

non-coronary obstructive ischemic heart disease

Interventions

Experimental group:Take Tongxinluo capsule
Control group:Nicodil was taken orally

Sponsors

Huadong Hospital affiliated to Fudan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Aged 18 to 75 years, No gender limitation; 2. Diagnostic criteria for stable angina: there was no change in the frequency, duration, cause or relief mode of angina attacks within the last 60 days;There was no evidence of recent myocardial injury; 3. CAG shows non-obstructive coronary arteries, including normal coronary arteries (stenosis < 30%) and mild stenosis (30% < Narrow < 50%); 4.CSF diagnostic criteria: correct TIMI frame Count (CTFC), that is, coronary blood flow from vessel opening to vessel terminal exceeds 27 frames when the angiographic image acquisition speed is 30 frames /s; 5. Evidence of myocardial ischemia: there is objective evidence of myocardial ischemia on ecg or radionuclide myocardial perfusion imaging in resting or exercise state.

Exclusion criteria

Exclusion criteria: 1. Severe aortic stenosis, hypertrophic obstructive cardiomyopathy, congestive heart failure, and malignant tumors; 2. Patients with a clear history of MI, PCI and CABG 6 months prior to screening; 3. Use of glucocorticoids within 3 months before screening; 4. Renal function impairment (serum creatinine >= 140µmol/L) or liver function impairment (ALT and/or AST >= 100IU/L).

Design outcomes

Primary

MeasureTime frame
Severity of angina pectoris;

Secondary

MeasureTime frame
Myocardial injury index (TnT, TnI, CK-MB);

Countries

China

Contacts

Public ContactHong Weilin

Huadong Hospital affiliated to Fudan University

shanghai_private_ryan@aliyun.com+86 13817732757

Outcome results

None listed

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