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Association between plaque progression and non-culprit healed plaque in ACS patients

Association between plaque progression and non-culprit healed plaque in ACS patients

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2100041924
Enrollment
Unknown
Registered
2021-01-10
Start date
2021-01-10
Completion date
Unknown
Last updated
2021-03-30

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

Conditions

coronary artery diseases

Interventions

non-culprit healed plaque group:Nil
non-culprit non-healed plaque:Nil

Sponsors

Chinese PLA General Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: Patients should meet all the following criteria to participate in the trial: 1.Receiving percutaneous transluminal coronary intervention with acute coronary syndrome; 2.Receiving intra-coronary optical coherence tomography; 3.Receiving repeated coronary angiography at a 6 to 18 months of follow-up; 4.With an age of 18 to 80 years old,regardless of gender; 5.Volunteering for the trial and signing the informed consent.

Exclusion criteria

Exclusion criteria: 1. Lesions from previous coronary artery bypass grafting; 2. lack of clear coronary angiogram; 3. insufficient length of OCT pull-back to cover the non-culprit lesions; 4. massive lumen thrombus or artifacts with sub-optimal imaging; 5. severe heart failure, chronic kidney failure or hypohepatia; 6. not proper to receive coronary angiography or OCT imaging; 7. pregnant or lactational women; 8. refused to receive visit or sign the consent.

Design outcomes

Primary

MeasureTime frame
minimum lumen diameter;

Secondary

MeasureTime frame
plaque features;

Countries

China

Contacts

Public ContactYundai Chen

Chinese PLA General Hospital

cyundai@vip.163.com+86 10-55499309

Outcome results

None listed

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