Nebivolol improves coronary flow reserve in patients with idiopathic dilated cardiomyopathy.
Dogan Erdogan, Hakan Gullu, Mustafa Caliskan...
https://pubmed.ncbi.nlm.nih.gov/17065184Actively Recruiting
Led by VZW Cardiovascular Research Center Aalst · Updated on 2025-07-14
46
Participants Needed
1
Research Sites
N/A
Total Duration
Researchers are evaluating whether beta-blockers can improve coronary blood flow and reduce resistance in patients with angina and no obstructive coronary arteries (ANOCA). This trial aims to answer if beta-blockers improve coronary blood flow and lower coronary microvascular resistance. The study compares a beta-blocker to a placebo in patients undergoing diagnostic angiography and found to have ANOCA, focusing on detailed coronary function measurements. Participants will be randomly assigned to receive either intravenous metoprolol, a beta-blocker, or a saline placebo. Before treatment, baseline measurements of coronary blood flow and resistance are taken using continuous intracoronary thermodilution, a precise method involving a pressure/temperature guidewire and infusion catheter. After administration, these measurements are repeated 10 minutes later to assess treatment effects. The procedure takes about 15 minutes and is performed under blinded conditions. During the study, participants undergo diagnostic angiography and detailed heart function tests including pressure and flow measurements at rest and during increased blood flow. Researchers measure parameters such as absolute coronary flow, microvascular resistance, epicardial resistance, coronary flow reserve, and myocardial perfusion. The study monitors changes from baseline to 10 minutes post-intervention to understand the impact of beta-blockers on coronary microvascular function and overall heart circulation.
CONDITIONS
Effect of Beta-blockers on Coronary Flow and Resistance in Patients With ANOCA
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Complete this quick 3-step screening to check your eligibility
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person) during diagnostic coronary angiography
Duration - Approximately 15 minutes
Participants receive a single intravenous dose of either beta-blocker (metoprolol) or placebo, and undergo detailed cardiovascular measurements before and 10 minutes after administration to assess the effect of the intervention on coronary flow and resistance.
1 visit (in-person) including baseline and post-intervention assessments
Total: 1 location
1
OLV Cardiovascular Center Aalst
Aalst, Flanders, Belgium, 9300
Actively Recruiting
A
Adriaan Wilgenhof, MD
T
Thabo Mahendiran, MD
Study Type
INTERVENTIONAL
Masking
QUADRUPLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
BASIC_SCIENCE
Number of Arms
2
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