INOCA (Ischemia With Non Obstructive Coronary Artery Disease)

2

Review clinical trials related to INOCA (Ischemia With Non Obstructive Coronary Artery Disease). Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

Advanced Invasive Diagnosis Strategy for Post-PCI Patients With Stable Coronary Syndromes Undergoing Coronary Angiography

AID Post-PCI Angina is as an observational, prospective, single-cohort, multicenter study designed to investigate the causes and origins of post-PCI angina by using the advance invasive diagnosis (AID) strategy combining with angiography derived physiology (ADP) in an all-comers population of patients with post-PCI angina referred for invasive coronary angiography. An all-comers population of patients with a history of previous percutaneous coronary intervention (PCI), who presented with angina or documented myocardial ischemia by non-invasive testing and are referred for invasive coronary angiography (ICA) will be enrolled. ICA will be performed with the application of the structure AID strategy to evaluate both obstructive and non-obstructive cause of myocardial ischemia. Then, angiography derived physiological assessment of epicardial coronary artery using functional coronary angiography in each vessel will be performed in both index procedure and the previous procedure in all patients. By combining information obtained from both procedures, the causes and origins of post-PCI angina will be made. Treatment will be decided by the operators according to the result. Patients will complete the Seattle Angina Questionnaire (SAQ) at baseline and at 1, 6, and 12 months after the procedure. The main hypothesis of this study states that, in patients with post-PCI angina referred to ICA, the application of the structured AID strategy combining with angiography derived physiology (ADP) will lead to a high diagnostic yield in identifying the origins of obstructive disease and causes of post-PCI angina.

Participants needed: 246
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Fundacion Investigacion Interhospitalaria CardiovascularUpdated: Jun 10, 2026Locations: 5Duration: 12 Months
Eligibility criteria

Patients with a history of previous percutaneous coronary intervention (PCI) wit...

Acute myocardial infarction (ST-segment elevation myocardial infarction [STEMI]... [+10]

Status: Recruiting

Analysis of Coronary Reactivity Testing With and Without Intracoronary Nitrate Testing

This single-arm, multi-center, prospective study will assess the coronary flow reserve (CFR), index of microcirculatory resistance (IMR), and determinants thereof (transit time, Pa, Pd) in patients before and after intracoronary nitroglycerine.

Participants needed: 50
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Baylor Research InstituteUpdated: May 5, 2026Locations: 1
Eligibility criteria

Aged 18 or older [+4]

Existing coronary artery disease [+5]