NCT06414265Toboroz
Reduction of Mitral Regurgitation With the SATURN Trans-Septal Transcatheter Mitral Valve Replacement (TMVR) System in Patients With Severe Symptomatic Mitral Regurgitation
Reduction or Elimination of Mitral Regurgitation With the SATURN Trans-Septal TMVR System in Patients With Severe Symptomatic Mitral Regurgitation - CASSINI-EU Trial
Forrás: ClinicalTrials.gov · Utoljára frissítve: 2026. máj. 20.
Rövid összefoglaló (regiszter, angolul)
The goal of this clinical trial is to evaluate feasibility, safety, and performance of the SATURN TS TMVR System for the treatment of moderate-to-severe or severe, symptomatic mitral regurgitation through a transcatheter approach. The main questions it aims to answer are: * is the use of the device feasible? * is it safe (defined as freedom from device-related major adverse events at 30 days)? * does it perform (defined as reduction of MR Grade to ≤ 1+ at 30 days)? Participants will need to do the following as part of the clinical trial: * complete 6-Minute Walking Test * complete Quality of Life Questionnaires * undergo blood evaluations * CT scan * 12 lead ECG * Transesophageal Echocardiography * Transthoracic Echocardiogram * the study procedure (valve implantation, right heart catheterization, left arterial pressure, fluoroscopy/ angiogram)
- Állapot (regiszter)
- Toboroz
- Vizsgálattípus
- Beavatkozással járó
- Résztvevők száma
- 30 (tervezett)
- Első benyújtás
- 2024. ápr. 29.
- Kezdés
- 2024. ápr. 4.
- Elsődleges befejezés
- 2027. márc.
- Fő szponzor
- InnovHeart
- Betegségek
- Szívelégtelenség
- NCT-szám
- NCT06414265
Mit vállalsz
- Vizsgálat típusa: Beavatkozással járó
- Tervezett résztvevők: 30
- 2024. ápr. 4. és az elsődleges befejezés (2027. márc.) között
- 8 helyszín, 5 országban
- Vizitek és vizsgálatok: kérdezd a vizsgálat csapatát, a regiszter nem sorolja fel őket
A(z) ClinicalTrials.gov regisztermezőiből összeállítva. A vizsgálat felépítését írja le.
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Korábbi kezelés
- Endocarditis in the 3 months prior to procedure date.
- COPD 2 on home oxygen therapy deemed too high risk for intubation.
- Myocardial infarction during prior 30 days.
- Stroke or TIA during prior 90 days.
- Severe extracardiac arteriopathy (safety measure for extra-circulatory support if surgical conversion is needed).
- Prior mitral valve treatment (e.g., valve repair or replacement, MitraClip, etc.), and/or anticipated mitral valve treatment prior to enrollment.
- Prior surgical mechanical valve AVR.
- Prior TAVI.
- CRT or ICD implanted in previous 30 days.
- CABG or PCI within previous 30 days.
- Prior or planned heart transplantation (UNOS status 1).
Más betegség
- Excessive frailty or comorbid conditions that preclude the anticipated benefit of the mitral valve replacement.
- Life expectancy <1 year due to noncardiac conditions.
- Current admission with acute heart failure exacerbation.
- Active systemic infection.
- Severe pulmonary arterial hypertension (PAH), defined as PASP > 60mmHg.
- Documented bleeding or coagulation disorders (hypo- or hyper-coagulable states).
- Severe connective tissue disease under chronic immunosuppressive or cortisone therapy.
- Need for any planned cardiovascular surgery or intervention (other than for MV disease) within 30 days post-index procedure.
- Inadequately treated for cardiac condition per applicable standards, such as for coronary artery disease, left ventricular dysfunction, mitral regurgitation, or heart failure, as reviewed by the Patient Screening Committee.
- Physical evidence of right-sided congestive heart failure:
- Patients with ascites.
- Patients with anasarca (generalized edema / hydropsy).
- Hypertrophic cardiomyopathy, restrictive cardiomyopathy, constrictive pericarditis, or other structural heart disease causing heart failure with the exception of dilated ischemic or non-ischemic cardiomyopathy.
- Procedural Exclusion Criteria
- Known hypersensitivity or contraindication to procedural or post-procedural medication (e.g., contrast solution, anticoagulation therapy).
- Documented hypersensitivity to nickel or titanium.
- Contraindications to TEE imaging
- Cardiac Imaging Exclusion Criteria
Laborértékek
- Chronic renal failure defined as eGFR <30 mL/min/m2 or on renal replacement therapy.
- Platelets < 90,000.
Egyéb
- General Exclusion Criteria
- Degenerative (i.e. intrinsic valve lesions) mitral regurgitation.
- Dependency on inotropic agents or mechanical circulatory support.
- Untreated clinically significant CAD.
- Modified Rankin Scale ≥4 disability.
- Refuses blood transfusions.
- Participating in other investigational studies likely to confound the results or affect the study.
- Unable or does not sign the study informed consent form.
- Patients classified as "vulnerable patients" 3 .
- Cardiovascular Exclusion Criteria
- Cardiogenic shock, hemodynamic instability, Systolic Blood Pressure <90mmHg, Inotropic dependent or requiring IABP/mechanical circulatory support.
- Left ventricular EF ≤ 30% by echocardiogram.
- Severe mitral annular calcification, severe mitral stenosis, valvular vegetation or mass.
- Extensive mitral flail leaflets
- Evidence of new or untreated intracardiac thrombus, mass, or vegetation.
- Severe right ventricular dysfunction.
- Severe tricuspid regurgitation.
- Hemodynamically significant inter-atrial shunt (ASD).
- Severe aortic regurgitation or aortic stenosis.
- Anatomic ineligibility for SATURN TS Bioprosthetic System or SATURN TS procedure as determined by the Screening Committee.
Kiket keres a vizsgálat
- Age 65 years or older.
- Symptomatic moderate to severe or severe functional mitral regurgitation (≥ Grade 3+).
- NYHA functional Class ≥ II. If Class IV, patient must be ambulatory.
- Ability to tolerate oral anticoagulation.
- Ability to qualify for bailout surgery (which may include open heart surgery).
- High risk for open-heart mitral valve surgery due to age, co-morbidities or frailty, as determined by the Heart Team.
- Willing and able to complete study-related assessments and questionnaires.
Életkor a regiszterben: 65 év – - · Nem: nők és férfiak · Egészséges önkénteseket nem fogad
Helyszínek (8)
Helyszínek a regiszter sorrendjében. Ha a profilodba mented a városodat, távolság szerint rendeződnek.
| Helyszín | Város | Ország | Helyszín állapota |
|---|---|---|---|
| Royal Sussex County Hospital | Brighton | Egyesült Királyság | Toboroz |
| Tbilisi Heart Center | Tbilisi | Grúzia | Toboroz |
| Tbilisi Heart and Vascular Clinic | Tbilisi | Grúzia | Toboroz |
| Instituto Clinico Humanitas | Milan | Olaszország | Toboroz |
| Ospedale San Raffaele | Milan | Olaszország | Toboroz |
| Vilnius University Hospital Santaros Klinikos | Vilnius | Litvánia | Toboroz |
| Gornoslaskie Centrum Medyczne | Katowice | Lengyelország | Toboroz |
| Warsaw Medical University | Warsaw | Lengyelország | Toboroz |
Ez az oldal tájékoztatás, nem orvosi tanács. Bármely vizsgálatról az orvosoddal beszélj.