NXT-ASSESS: A Study for Exploring the Efficacy of Naoxintong Capsules in the Treatment of Coronary Atherosclerotic Plaque on the Basis of Optimal Medical Therapy (Aspirin,Statins,Clopidogrel, Etc.): Stage One
Study Details
Study Description
Brief Summary
To evaluate and compare the change of plaque composition by VH-IVUS imaging in subjects who take NXT and placebo in post-PCI of AMI patients during 12 months follow-up.
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
|
N/A |
Detailed Description
NXT-ASSESS is a placebo controlled,double-blind,randomised trial for assessment of the efficacy of Naoxingtong capsules in the treatment of coronary atherosclerotic plaque in patients with acute myocardial infarct on the basis of optimal medical therapy.A total of approximately 80 AMI patients with selective PCI indication who take NXT and placebo in post-PCI 12 months
Study Design
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| Experimental: Naoxintong Capsule Naoxintong Capsule |
Drug: Naoxintong Capsule
Patients with acute myocardial infarct on the basis of optimal medical therapy will take Naoxintong capsules following directions for 12 months
|
| Placebo Comparator: Placebo Placebo |
Drug: Placebo
Patients with acute myocardial infarct on the basis of optimal medical therapy will take placebo following directions for 12 months
|
Outcome Measures
Primary Outcome Measures
- Plaque composition [12 months]
The change of plaque composition by virtual histology intravascular ultrasound imaging in subjects who take Naoxintong capsules and placebo in post-percutaneous coronary intervention follow-up
- Plaque fibrous cap thickness [12 months]
The change of plaque fibrous cap thickness measured by optical coherence tomography in subjects who take Naoxintong capsules and placebo during post-percutaneous coronary intervention follow-up
Secondary Outcome Measures
- Lipid arc [12 months]
The change of lipid arc measured by optical coherence tomography in subjects who take Naoxintong capsules and placebo in post-percutaneous coronary intervention follow-up
- Percent atheroma volume [12 months]
The change of percent atheroma volume measured by intravascular ultrasound imaging in subjects who take Naoxintong capsules and placebo capsules during post-percutaneous coronary intervention follow-up
- Total atheroma volume and low attenuation plaque volume [12 months]
Total atheroma volume and low attenuation plaque volume measured by Coronary-CTA in subjects who take Naoxintong and placebo capsules during post-percutaneous coronary intervention follow-up
- Lipid [12 months]
The change of lipid measured by optical coherence tomography in subjects who take Naoxintong capsules
- Platelet function [12 months]
The change of platelet function measured by optical coherence tomography in subjects who take Naoxintong capsules
- Clinical incidents [12 months]
The number of clinical incidents in subjects who take Naoxintong capsules
- Culprit vessel [12 months]
The change of subjects culprit vessel with optical coherence tomography;
Eligibility Criteria
Criteria
Inclusion Criteria:
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Signing informed consent;
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Male or female aged 18 to 75 years old;
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AMI patients with selective PCI indication primary PCI patients are exclusive;
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No history of CABG or PCI;
Image inclusion criteria:
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CCTA at least one in-segment ≥20% and ≤70% diameter stenosis non-culprit vessel in the proximal-middle segments of RCA, LCX, LAD (the proximal and distal plaque within 5mm, same as below);
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Radiography diameter of target vessel, 2.5-4.0mm;
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Studied vessel can be evaluated with OCT and IVUS; OCT: the visual target study lesion is lipid-rich plaque with lipid arc≥100 degree and fiber cap thickness≤120µm.
Exclusion Criteria:
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Life expectancy is less than 1 year;
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Cannot implant drug stent;
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Received ≥4weeks systematic treatment of statin and other lipid-lowering drug in the 3 months before admission;
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Received ≥4 weeks systematic treatment of any traditional Chinese medicine;
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Known to have adverse reaction to ingredients of NXT capsule;
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Patients with severe heart disease that CABG or selective PCI, heart transplantationSAVR/TAVR are required during the study(12 months);
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LVEF<40%;
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Drug uncontrollable recurrent and highly symptomatic arrhythmia such as ventricular tachycaidia, atrial fibrillation with rapid ventricular rate and paroxysmal supraventricular tachycardia in the 3 months before ACS admission;
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Known any stroke;
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Other operations arranged during the study period (12 months);
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Uncontrollable hypertension, defined as resting systolic BP≥180mmHg;
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Clinical confirmed as statin intolerance;
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Type I diabetes or type 2 diabetes that is not well controlled;
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Moderate and severe renal dysfunction (defined as eGFR<30ml/min/1.73m2);
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Clinical confirmed liver disease or liver dysfunction (AST or ALT >3*ULN);
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Clinical confirmed infection and other hematological, metabolic gastrointestinal or endocrine dysfunction that researchers believe not suitable for enrollment;
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Known factors that may not be compliant, such as alcoholism, drug addiction, mental illness, etc.;
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Participated in other clinical research projects, or within 30 days of the last participating clinical project;
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Pregnant,breast feeding women or those plan to conceive during the study;
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History of malignant tumor.
Lesion related:
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Target segment severe calcification;
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Failed PCI in culprit vessel;
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Failed OCT screening (lipid arc/ fiber cap thickness does not match filter criteria);
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Complications during the evaluation of OCT and IVUS/VH-IVUSOCT and IVUS/VH-IVUS evaluation failed due to instruments.
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | Chinese Academy of Medical Sciences, Fuwai Hospital | Beijing | Beijing | China | 100010 |
Sponsors and Collaborators
- Chinese Academy of Medical Sciences, Fuwai Hospital
Investigators
None specified.Study Documents (Full-Text)
None provided.More Information
Publications
None provided.- CRFH20180010