Acute Coronary Syndrome Clinical Trials

Find Acute Coronary Syndrome Clinical Trials Near You

Single Antiplatelet Treatment With Ticagrelor or Aspirin After Transcatheter Aortic Valve Implantation: Multicenter Randomized Clinical Trial

Status: Recruiting
Location: See location...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Phase 4
SUMMARY

The optimal pharmacological therapy after transcatheter aortic valve implantation (TAVI) to prevent valve thrombosis and reduce thromboembolic complications without significantly increasing the risk of bleeding is not yet fully defined and constitutes an important unmet clinical need. Recently, single antiplatelet therapy (SAPT) with Aspirin has been increasingly adopted to avoid bleeding early after TAVI compared with dual antiplatelet therapy. However, TAVI population is affected by a diversity of chronic pathologies that increase the risk of post-TAVI ischemic complications. Stroke is prevalent, especially peri- and early post-TAVI (\<1-8% in the 1st year). Although peri-TAVI myocardial infarction (MI) is rare (1-3%), concomitant coronary artery disease (CAD), diabetes mellitus (DM), and peripheral vascular disease (PVD), is very frequent in the TAVI population, affecting around 30-70% of patients. In patients with CAD, the need to re-access the coronary arteries after TAVI is challenging and can be hampered by the trancatheter valve struts. This is critical in TAVI patients with an acute coronary syndrome and in younger patients with long-life expectancy after TAVI. The use of a P2Y12 inhibitor provides significant ischemic protection in the in the coronary, cerebral and peripheral vascular territories compare to Aspirin. The use of a P2Y12 inhibitor as antiplatelet treatment can decrease the need for new coronary revascularizations and reduce the incidence of thromboembolic complications after TAVI.

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

• Provision of informed consent prior to any study specific procedures.

• Adult patients (more than 18 years) with ability to understand and accept the participation in the clinical trial.

• Patients with degenerative symptomatic severe aortic stenosis (AS) accepted for TAVI with any of the commercial approved TAVI devices after evaluation of the Heart Team of each center,and with at least one of the following comorbidities:

‣ Diabetes Mellitus, the current WHO diagnostic criteria for diabetes should be maintained - fasting plasma glucose ≥ 7.0mmol/l (126 mg/dl) or 2-h plasma glucose ≥ 11.1mmol/l (200mg/dl), or under treatment with an oral hypoglycemic or insulin.

⁃ Prior coronary artery disease (STEMI, NSTEMI, stable angina, or others) documented by invasive or non-invasive ischemia screening tests or imaging study.

⁃ Prior peripheral arterial disease documented by invasive or non-invasive ischemia screening tests or imaging study.

• Successful TAVI performed by any vascular access.

• Patients who are not participating in any other clinical trial or research study (registries allowed).

Locations
Other Locations
Spain
Hospital Alvaro Cunqueiro
RECRUITING
Vigo
Contact Information
Primary
Victor A Jiménez Díaz, MD, MPH
victor.alfonso.jimenez.diaz@sergas.es
+34986825564
Backup
Pablo Juan-Salvadores, Pharma, MPH, PhD
pablo.juan.salvadores@sergas.es
+34986825564
Time Frame
Start Date: 2022-01-21
Estimated Completion Date: 2028-06-30
Participants
Target number of participants: 1206
Treatments
Active_comparator: Acetylsalicylic acid 100mg/day
Aspirin 100 mg/day after TAVI
Experimental: Ticagrelor 60mg twice per day
Ticagrelor 60 mg twice per day after TAVI
Sponsors
Leads: Fundacin Biomedica Galicia Sur

This content was sourced from clinicaltrials.gov

Similar Clinical Trials