COronary CoLLateralization in Type 2 diabEtic Patients With Chronic Total Occlusion
- Conditions
- Chronic Total Occlusion of Coronary ArteryDiabetes Mellitus, Type 2
- Registration Number
- NCT06054126
- Lead Sponsor
- Ruijin Hospital
- Brief Summary
A severe coronary artery obstruction is a prerequisite for spontaneous collateral recruitment. The formation of coronary collateral circulation(CCC) is significantly impaired in type 2 diabetic patients with chronic total occlusion (CTO) compared with non-diabetic patients with CTO. This retrospective cohort enrolls consecutive T2DM patients who had at least one lesion with coronary angiographic total occlusion.
- Detailed Description
COronary CoLLateralization in Type 2 diabEtic Patients With Chronic Total Occlusion (COLLECT) study is a single center, retrospective cohort study to investigate potential factors associated with the development of coronary collateral circulation in diabetic patients. Investigators will consecutively enroll T2DM patients who had at least one lesion with coronary angiographic total occlusion. The development of coronary collateral circulation will be graded according to the Rentrop method and patients will be divided into poor CCC (grade 0 or 1) or good (grade 2 or 3) CCC groups according to their Rentrop grades. Baseline clinical and laboratory characteristics at hospital admission will be recorded to analyze potential factors associated with the development of coronary collateral circulation in T2DM patients with CTO. Later, their cardiac function will be evaluated by echocardiography at one year follow-up.
Recruitment & Eligibility
- Status
- RECRUITING
- Sex
- All
- Target Recruitment
- 2000
- Age 18-90 years
- Type 2 diabetes diagnosed by one of the following criteria:
HbA1c >/= 6.5% Fasting plasma glucose >/= 7.0 mmol/l (confirmed) 2h plasma glucose value during OGTT >/= 11.1 mmol/l Already receiving glucose-lowering agents.
- At least one lesion with angiographic total occlusion
- eGFR<15mL/(min·1.73m2)
- chronic heart failure with NYHA grade ≥3
- had a history of coronary artery bypass grafting
- had received a percutaneous coronary intervention within the prior 3 months
- Malignant tumor or immune system disorders
- Pulmonary heart disease
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Cardiac function evaluated by echocardiography 12 months Assessed by echocardiography
- Secondary Outcome Measures
Name Time Method Cardiovascular events up to 5 years The incidence of MACCE (major adverse cardiac and cerebrovascular events)
Trial Locations
- Locations (1)
Ruijin Hospital, Shanghai Jiao Tong University School of Medicine
🇨🇳Shanghai, Shanghai, China
Ruijin Hospital, Shanghai Jiao Tong University School of Medicine🇨🇳Shanghai, Shanghai, ChinaYing ShenContact18601683266rjshenying@qq.com