- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06237244
Insulin Resistance Indices and Coronary Artery Disease
Predicting the Presence and Severity of Coronary Artery Disease Using Surrogate Markers of Insulin Resistance: A Cross-Sectional Study
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
This was an analytical cross-sectional retrospective study involving patients with suspected CAD who underwent coronary angiography between December 2018 and May 2023. The information was obtained from patients referred to the outpatient cardiovascular clinic (Professor Kojuri Cardiology Clinic, Shiraz, Iran, www.kojuriclinic.com). Data was extracted from Professor Kojuri Cardiology Clinic database, including patient's information about the clinical history, presence or absence of specific diseases, angiography/angioplasty results, medications, and laboratory values.
A total of 14,708 patients who had undergone coronary angiography at least once were examined. After applying exclusion criteria, 1017 eligible cases were selected for data analysis.
The following data was recorded for the included patients: demographic data, past medical history (such as DM, hypertension, etc.), systolic and diastolic blood pressure, weight and height, fasting plasma glucose (FPG), hemoglobin A1c (HbA1c), total cholesterol (TC), triglyceride (TG), low-density lipoprotein cholesterol (LDL-C), high-density lipoprotein cholesterol (HDL-C), and serum creatinine (Cr). Body mass index (BMI) was calculated as weight (Kg) divided by the square of height (m2). Obesity was defined as BMI ≥ 30 Kg/m2.
Laboratory values were selected from the time before angiography, and if not available, from the time shortly after the angiography. This helped us find those values which could best represent the metabolic state of patients at the time of angiography, while reducing the confounding effect of statin use.
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
-
-
Fars
-
Shiraz, Fars, Iran, Islamic Republic of, 7134814336
- Shiraz University of Medical Sciences
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- patients with age more than 18 years and having undergone coronary angiography
Exclusion Criteria:
- incomplete data
- history of prior coronary angiography or revascularization (percutaneous coronary intervention (PCI) or coronary artery bypass grafting (CABG))
- serum creatinine > 1.4 mg/dL
- history of chronic kidney disease (CKD)
- cancer,
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
coronary artery disease
patients with coronary angiography of at least one vessel with more than 50% stenosis
|
Ratio of triglyceride level to glucose
Ratio of triglyceride to HDL cholesterol
|
|
no coronary artery disease
patient with no stenosis in coronary angiography
|
Ratio of triglyceride level to glucose
Ratio of triglyceride to HDL cholesterol
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
insulin resistance index: level of triglyceride to glucose ratio from blood sample
Time Frame: 3 years
|
correlation of coronary artery disease and triglyceride glucose ratio in blood laboratory tests
|
3 years
|
|
insulin resistance index: Level of triglyceride to HDL ratio from blood sample
Time Frame: 3 years
|
correlation of coronary artery disease and triglyceride to HDL level ratio in blood laboratory sample
|
3 years
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
metabolic syndrome
Time Frame: 3 years
|
metabolic syndrome based on criteria of metabolic syndrome
|
3 years
|
Collaborators and Investigators
Investigators
- Principal Investigator: Javad Kojuri, MD. MS., professor Kojuri cardiology clinic
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- IR.SUMS.MED.REC.1402.252
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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