INOCA Spanish National Registry: ESP-INOCA

Status: Recruiting
Location: See all (3) locations...
Study Type: Observational
SUMMARY

Coronary atherosclerosis is the most common cause of ischaemic heart disease. About 40-50% of patients with symptoms and documented ischaemia on non-invasive tests do not show obstructive coronary artery disease on coronary angiography. This cause of ischaemic heart disease called INOCA (Ischemic Non-Obstructive Coronary Artery), far from having a benign prognosis, is associated with an increase in major adverse cardiac events (MACE) as well as increased functional limitation. The current European Society of Cardiology clinical practice guidelines for the management of chronic coronary syndrome establish for the first time a IIa recommendation for the invasive analysis of coronary flow reserve (CFR) and microvascular resistance index (MRI) in symptomatic patients with INOCA. The acetylcholine (Ach) test, based on intracoronary (ic) administration, is established as indication IIb for the assessment of micro or macrovascular vasospasm in patients with suspected vasospastic angina (VSA) (4). A national multicentre registry would allow us to determine the prevalence of INOCA and its different endotypes in our setting.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Patients \> 18 years.

• Anginal symptoms.

• Anginal equivalent with positive myocardial ischaemia test.

• Absence of obstructive coronary artery disease (diameter stenosis \<50% or \>50% with a FFR\>0.80).

• Patients undergoing invasive coronary function test.

• Signed informed consent.

Locations
Other Locations
Spain
Hospital Universitario de la Princesa
RECRUITING
Madrid
Hospital Universitario Virgen de Arrixaca
RECRUITING
Murcia
Hospital General Universitario de Valencia
RECRUITING
Valencia
Contact Information
Primary
Eva Rumiz, MD, PhD
evarumizgonzalez@gmail.com
+34 963131800
Time Frame
Start Date: 2024-03-24
Estimated Completion Date: 2026-03
Participants
Target number of participants: 1000
Related Therapeutic Areas
Sponsors
Collaborators: Hospital Clinic of Barcelona, Hospital Universitario 12 de Octubre, Hospital Universitario La Fe, Hospital General Universitario de Alicante, University Hospital Gregorio Marañón, Hospital Universitario La Paz, Hospital General Universitario Elche, Hospital Universitario San Juan de Alicante, Hospital de la Ribera, Hospital Universitario Puerta del Mar, Hospital Clinico Universitario de Santiago, Hospital San Carlos, Madrid, Complejo Hospitalario Universitario de Huelva, Hospital de Basurto, Hospital Universitario Ramon y Cajal, Hospital Universitario Virgen de la Arrixaca, University of Salamanca, Hospital Miguel Servet, Hospital de Manises, Hospital Donostia, Complexo Hospitalario Universitario de A Coruña, Hospital Universitario Marqués de Valdecilla, Hospital Universitari de Bellvitge, Hospital Universitario de Torrevieja, Hospital Clínico Universitario Lozano Blesa, Hospital Clínico Universitario de Valladolid, Hospital Clínico Universitario de Valencia, Puerta de Hierro University Hospital, Hospital Universitario Virgen del Rocio, Fundación de Investigación Biomédica - Hospital Universitario de La Princesa, Hospital Virgen de la Salud, University Hospital of the Nuestra Señora de Candelaria, Hospital Universitario Fundación Jiménez Díaz, Hospital de la Santa creu i Sant Pau - Barcelona, Hospital General Universitario de Castellón
Leads: Eva Rumiz González

This content was sourced from clinicaltrials.gov