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Comparison of Vascular Remodeling Between Different Antianginal Medication Evaluated by Noninvasive ECG-gated Fundus Photographic Evaluation

Comparison of Vascular Remodeling Between Different Antianginal Medication Evaluated by Noninvasive ECG-gated Fundus Photographic Evaluation

Status
UNKNOWN
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01162902
Enrollment
150
Registered
2010-07-15
Start date
2013-09-30
Completion date
2015-12-31
Last updated
2013-12-17

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

Conditions

Stable Angina

Brief summary

Treatments for stable angina includes drug therapy such as calcium-channel blocker, beta blocker, and ACEI/ARB. To obtain good prognosis in patients with coronary artery disease,preventing or correcting the progression of atherosclerosis and dyslipidemia is more important than relieving angina symptom. Dysfunction of microvessel is one of the most important factor in patients with coronary artery disease. Recently, we developed the new non-invasive method of evaluating the microvessel in fundus. With this methods, we will compare the effect of each drug (beta blocker, CCB, ARB).

Interventions

DRUGDiltiazem treated group

Diltiazem 180mg for 9 months

DRUGBisoprolol treated group

Bisoprolol 5mg for 9 months

DRUGCandesartan treated group

Candesartan 32mg for 9 months

Sponsors

Seoul National University Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
30 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

* Stable angina patients whose coronary lesions is confirmed by angiography or receives PCI * Unstable Angina/NSTEMI patients who completed PCI for main lesions * Either systolic \> 130mmHg or diastolic \> 80mmHg, or patients with anti-hypertensive drugs

Exclusion criteria

* STEMI patients within one month * Variant Angina * Liver function abnormality or renal failure * History of Hypersensitivity to testing drugs * Severe heart failure(NYHA class\>3) or uncorrectable hematologic disease * Woman possible to be pregnant * Uncontrolled diabetes * Expected life span \< one year

Design outcomes

Primary

MeasureTime frameDescription
Wall to lumen ratio of fundus vesselbaseline, 9 monthsMeasurement of change in the ratio of wall thickness to lumen of the fundus vessel from baseline to 9 month follow up

Secondary

MeasureTime frameDescription
lipid parameterbaseline, 9 monthsMeasurement of change in total cholesterol, triglyceride, LDL, small dense LDL, and HDL
Serum markers of inflammationbaseline, 9 monthsCRP
Change of nitrate needbaseline, 1 months, and 3 monthsMeasure of change of nitrate need

Countries

South Korea

Contacts

Primary ContactHae-Young Lee, MD, PhD
hylee612@snu.ac.kr82-10-4528-6160
Backup ContactHyo-Soo Kim, MD, PhD
hyosoo@snu.ac.kr82-2-2072-2226

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026