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A randomized controlled clinical study of blood lipid levels predicting immediate and long-term outcomes after interventional therapy

A randomized controlled clinical study of blood lipid levels predicting immediate and long-term outcomes after interventional therapy

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400085885
Enrollment
Unknown
Registered
2024-06-20
Start date
2024-06-20
Completion date
Unknown
Last updated
2024-07-08

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

Conditions

coronary artery disease

Interventions

DCB:drug-coated balloons
DES:drug-eluting stents

Sponsors

Yellow River Sanmenxia Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: Selected criteria that comply with coronary arterial intervention therapy (according to the "Guidelines for the Treatment of Cross -Coronatte Artelis in China in 2021"), which belongs to · Protonous coronary arteries · Reference blood vessel diameter =2.0 mm and =4 mm · No severe calcification · The narrow diameter of the thrombosis and pre -expansion of the thrombosis does not exceed 50%(visual inspection)

Exclusion criteria

Exclusion criteria: 1) Age 80 years old 2) Known in intracranial diseases (lumps, aneurysm, dynamic vein malformation, hemorrhagic CVA, ischemic CVA/TIA <6 months ago, including or ischemia, (permanent nerve dysfunction) 3) Known taboos: Bidamu, sodium sodium sodium, heparin, aspirin, Praograi/or Tetkagrai 4) Pure/ventilation 5) Severe heart failure (NYHA heart function =III) or left ventricular ejection score <35% 6) Heartogenic shock 7) Bleeding risk is high (patients with a CRUSADE score standard exclude patients with high risks above the risk of risk) 8) The expected life span is less than 12 months 9) Unable to provide informed consent 10) Other researchers believe that it is not suitable for participating in the situation of this study

Design outcomes

Primary

MeasureTime frame
major adverse cardiovascular events;

Secondary

MeasureTime frame
Target lesion revascularization;Target vessel revascularization;Target vessel failure;All-cause mortality;Cardiac mortality;Myocardial infarction;In-stent thrombosis;

Countries

China

Contacts

Public ContactLi Zheng

Yellow River Sanmenxia Hospital

vera_well4@hotmail.com+86 159 7833 7541

Outcome results

None listed

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