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NCT05278182: NXT-ASSESS

A Placebo Controlled, Double-blind, Randomised Trial for Assessment of the Efficacy of Naoxintong Capsules in the Treatment of Coronary Atherosclerotic Plaque in Patients With Acute Myocardial Infarct on the Basis of Optimal Medical Therapy (Aspirin,Statins, Clopidogrel, Etc.)

Status unknown NA Last updated 18 May 2022
What this trial tests

NA trial testing Naoxintong Capsule in Atherosclerotic Cardiovascular Disease in 80 participants. Status unknown.

Timeline
1 December 2022
Primary endpoint
30 June 2025
30 June 2025

Quick facts

Lead sponsorChinese Academy of Medical Sciences, Fuwai Hospital
PhaseNA
StatusStatus unknown
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingsingle
Primary purposetreatment
Enrollment80
Start date1 December 2022
Primary completion30 June 2025
Estimated completion30 June 2025
Sites1 location across China

Drugs / interventions tested

Conditions studied

Sponsor

Chinese Academy of Medical Sciences, Fuwai Hospital

Who can join

Adults 18 to 75, any sex, with Atherosclerotic Cardiovascular Disease. Patients with the condition only — healthy volunteers not accepted.

What's being measured

Primary outcomes are the specific endpoints the trial is designed to prove or disprove.

Sponsor's own description

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.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Atherosclerotic Cardiovascular Disease

Currently open trials in the same condition.

Other Chinese Academy of Medical Sciences, Fuwai Hospital trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT05278182.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing