First prospective randomized trial to examine a differential therapeutic response in symptomatic patients with non-obstructive coronary artery disease after coronary physiological testing (EXAMINE-CAD-DZHK22)

ID

NCT05294887

Status

Active

DZG

DZHK

Start date

03/04/2022

Parameters

Inclusion criteria
  • Age 18 - 85 years Recurrent angina symptoms provoked by exercise and/or repeated attacks of angina at rest (both at least for 4 weeks) Absence of flow-limiting coronary artery stenosis (as defined by any coronary artery diameter reduction >50% or fractional flow reserve ≤0.80) Left ventricular ejection fraction (LVEF) >50% Written informed consent
Exclusion criteria
  • Pregnancy
  • planned pregnancy
  • or breast-feeding Female patients of childbearing potential who are unwilling to use a highly effective contraception method during trial participation according to CTFG. In addition
  • a negative serum or urine pregnancy test must be available prior to randomization. Expected life expectancy <1 year Contraindications to withholding nitrates
  • calcium channel blockers
  • and beta blockers for 48 hours before invasive coronary reactivity testing (e.g. clinical need for rate control in case of permanent atrial fibrillation
  • recurrent angina symptoms without any possibility to wihthold ongoing medication) Known hypersensitivity or contraindication to bisoprolol or diltiazem or any of its excipients. Concomitant therapy with systemic drugs that are strong inhibitors of both CYP3A4 and P-gp (azole antimycotics such as ketoconazole and itraconazole or HIV protease inhibitors such as ritonavir) Concomitant therapy with drugs that are strong CYP3A4 inducers (e.g. carbamazepine
  • phenytoin
  • rifampicin
  • St. John's wort) Bradycardia (<50/min) at time of randomization Symptomatic hypotension (<100 mmHg) at time of randomization Cardiogenic shock Second and third degree atrioventricular block
  • sick sinus syndrome
  • sinoatrial block Severe valvular heart disease (grade III) Any cardiomyopathy including those with preserved left ventricular ejection fraction (LVEF) Chronic obstructive pulmonary disease Severe bronchial asthma Metabolic acidosis at time of randomization Renal failure (creatinine >2.0 mg/dL) N-terminal pro B-type natriuretic peptide (NT-proBNP) >300 ng/L Known significant liver disease (e.g. acute hepatitis
  • chronic active hepatitis
  • cirrhosis) which is associated with moderate or severe hepatic impairment (alanine aminotransferase (ALT) and/or aspartate aminotransferase (AST) ≥2.0 upper limit of normal (ULN)) Untreated pheochromocytoma Late stage of peripheral arterial disease or Raynaud's syndrome Participation in another clinical trial according to AMG or MPG at the time of randomization and the duration of this trial Patients who are unwilling to consent to saving and propagation of pseudonymized medical data for study reasons Persons who are legally detained in an official institution Persons likely to not be available to complete all protocol-required study visits or procedures
  • and/or to comply with all required study procedures to the best of patient's and investigator's knwoledge Persons who may dependent on the Sponsor
  • the Investigator or the trial sites
  • are not eligible to enter the trial Active coronavirus disease 2019 (COVID-19) at time of randomization