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COronary CoLLateralization in Type 2 diabEtic Patients With Chronic Total Occlusion

Recruiting
Conditions
Chronic Total Occlusion of Coronary Artery
Diabetes 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
Inclusion Criteria
  • 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
Exclusion Criteria
  • 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
NameTimeMethod
Cardiac function evaluated by echocardiography12 months

Assessed by echocardiography

Secondary Outcome Measures
NameTimeMethod
Cardiovascular eventsup 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, China
Ying Shen
Contact
18601683266
rjshenying@qq.com

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