FIH Study of the GEMINUS TAVI System in Patients With Severe Symptomatic Aortic Stenosis

Valve Medical

Status

Enrolling

Conditions

Aortic Valve Stenosis

Treatments

Device: GEMINUS Transcatheter Aortic Valve Implantation system

Study type

Interventional

Funder types

Industry

Identifiers

NCT05909748

GEMINUS-001

Details and patient eligibility

About

The main objective of this study is to evaluate the feasibility and safety of the GEMINUS system in patients with severe symptomatic aortic stenosis.

This is a prospective, open label, multicentre, single arm, first in human clinical study.

Clinical follow up for all patients will be performed at 30 days, 6 months, 1, 2, 3, 4 and 5 years post-implantation

Enrollment

30 estimated patients

Sex

All

Ages

18 to 120 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Age ≥ 18 years
Patient understands the implications of participating in the study and provides informed consent
Patient is willing to comply with specified follow-up evaluation
Severe aortic stenosis as per ACC/AHA 2020 guidelines (e.g. AVA ≤ 1.0 cm2 (or AVA index ≤ 0.6cm2/m2)* AND PV ≥ 4 m/sec or mean gradient ≥ 40 mmHg)** as determined by TTE/CT-TAVI

*May be larger with mixed AS/AR

**For low flow low gradient AS or paradoxical low flow severe AS must meet ACC/AHA guidelines (table 13 stages of AS in the guideline)
Cardiac Symptoms: ≥ NYHA Class II
Patient ≥ intermediate surgical risk as assessed by the heart team or ≥75 years old.
Aortic annulus diameter ≥22 mm and < 29 mm, assessed by CT TAVI
Anatomically suitable for implantation of the GEMINUS device
Peripheral vessels (common femoral and iliac arteries) of acceptable size (minimal diameter > 4mm), tortuosity, and calcification to accommodate the 12Fr catheter system.
Patients assessed by the heart team to be at high risk for access site related bleeding/vascular complications due to the caliber/ calcification/ atherosclerosis of the iliofemoral vessels.

Exclusion criteria

Patient not suitable for surgical bailout
Congenital uni/bi/quadricuspid valve, or noncalcified aortic valve.
Mixed aortic valve disease (aortic stenosis and aortic regurgitation with predominant aortic regurgitation ≥3+).
Active or recent (within 6 months) endocarditis.
Active systemic infections.
Recent MI (≤ 1 month).
Any therapeutic invasive cardiac procedure (except BAV) performed within 30 days of the index procedure.
Prosthetic heart valve in any position.
Severe (> 3+) mitral, tricuspid or pulmonic regurgitation.
Blood dyscrasias as defined: leukopenia (WBC<3000/mm3), acute anemia (Hb <8mg%), thrombocytopenia (platelet count <50,000 cells/mm3), history of bleeding diathesis or coagulopathy.
Untreated clinically significant coronary artery disease requiring revascularization.
Hemodynamic instability requiring inotropic support or mechanical support devices.
Hypertrophic cardiomyopathy with or without obstruction (HCM).
Severe ventricular dysfunction with left ventricular ejection fraction (LVEF) <20%.
Echocardiographic evidence of intracardiac mass, thrombus or vegetation.
Active peptic ulcer or upper GI bleeding within the prior 3 months.
Known hypersensitivity or contraindication to heparin, inability to tolerate antiplatelet therapy or sensitivity to contrast media (which cannot be adequately premedicated).
Recent (<6 months) cerebrovascular accident (CVA) or transient ischemic attack (TIA).
Renal insufficiency (eGFR<30 mL/min) and/or end stage renal disease requiring chronic dialysis.
Severe aortic disease, including abdominal aortic or thoracic aneurysm (lumen diameter > 5cm), marked tortuosity, or severe aortic arch atheroma.
Life expectancy < 12 months due to non-cardiac co-morbid conditions.
Currently participating in an investigational drug or another device study that has not reached its primary endpoint