NCT05172960ClinicalTrials.gov

ALLIANCE: Safety and Effectiveness of the SAPIEN X4 Transcatheter Heart Valve

Safety and Effectiveness of Balloon-Expandable Bioprosthetic SAPIEN X4 Transcatheter Heart Valve

מגייסמקבל משתתפים כעת, לפי רשומת המרשם.

יצירת קשר עם המחקר

בקצרה

The objective of this study is to establish the safety and effectiveness of the Edwards SAPIEN X4/X4S Transcatheter Heart Valve (THV) in subjects with symptomatic, severe, calcific aortic stenosis (AS).

התערבותידרושים 1,234 משתתפים65 אתרים4 מדינות

קטגוריות

לב וכלי דם100%

רשום במרשם אחד

ClinicalTrials.govNCT05172960פתיחת רשומה זו ב־ClinicalTrials.govסונכרן לפני 3 שבועות

מחקר יחיד יכול להיות רשום בכמה מרשמים. אנו מציגים אותו פעם אחת ומקשרים לכל רשומה שברשותנו.

מידע הניסוי מוצג כפי שפורסם על ידי המרשם, בשפת המקור שלו.

מתעניינים במחקר הזה?

התחברות או צרו חשבון כדי לרשום את התעניינותכם ולעקוב אחר המחקר הזה.

How this study is set up

The points below are drawn from the public registry record for this study. Each one cites the field or sentence it came from. A dash (—) means the record does not state something — not that it is missing or wrong. Many well-run studies, especially small ones, leave some of these blank.

Present: Registered before enrolment beganFirst posted 2021-12-29; recorded start 2022-06-20
Present: Has a defined primary outcomeA primary outcome measure is listed in the record
Present: The primary outcome states a time frameThe primary outcome measure records a time frame
Not stated: Participants are not randomly assignedAllocation is recorded as non-randomised
Present: Has a comparison groupThe record lists a placebo or comparator arm, or more than one study arm
Not stated: Open label (no blinding)Masking is recorded as none (open label)
Not stated: An ethics committee is not stated in the registry recordThis registry's ingested record has no ethics-committee field
Not stated: Regulatory oversight (such as an IND or IDE) is not stated in the registry recordThis registry's ingested record has no regulatory-authorisation field
Not stated: A data monitoring committee is not stated in the registry recordThis registry's ingested record has no data-monitoring-committee fieldA data monitoring committee is not required for many smaller studies, and its absence here is not unusual.
Present: No cost to participants is mentioned in the recordChecked the summary, description and eligibility text; no cost-to-participant phrase found
Present: Sponsor has 47 other studies in this databaseCounted from the lead sponsor named in the record (Edwards Lifesciences)
Present: Sponsor has posted results for at least one studyBased on the sponsor’s studies in this database

The record lists 1 condition.
Lead sponsor type recorded as: industry.

These are facts from the public registry record, not a judgement about the study. Discuss any trial with your own doctor before taking part.

What these facts mean, and what to ask · ruleset v1

Trial stature

Three independent measures of this study, described from its registry record — not a recommendation about it. A rigorous study by investigators nobody has heard of is better evidence than a weak study led by a famous one. How these are scored.

Methodological rigourMODERATE

A moderately rigorous design for a study of this type, judged from its ClinicalTrials.gov record.

How this score is built

Randomised allocation0/20
Non-randomised allocation
Blinding0/20
Open-label
Control arm0/15
No comparator arm stated in the record
Primary-outcome specificity10/10
Named primary outcome with a defined time frame
Endpoint type10/10
Mortality / MACE endpoint (hard clinical outcome)
Multi-centre8/8
Multi-centre: 65 sites
Data monitoring committee7/7
A data monitoring committee is in place
Prospective registration5/5
Registered before the study start date
Protocol / SAP posted0/5
No protocol or SAP posted to the registry

ScaleLARGE

A large study, international in scope: 1,234 participants (target), run at 65 sites, across 4 countries.

How this score is built

Enrolment31/40
1,234 participants (target)
Site count21/25
65 sites
Country count7/15
4 countries
Planned duration10/10
Planned over about 177 months
Sponsor scale6/10
Edwards Lifesciences has led 47 trials in our corpus

Investigator standingUNKNOWN

We have no verifiable track record for the investigator named on this trial. That is common for early-career investigators and for records held outside ClinicalTrials.gov — it is not a negative signal.

How this score is built

Investigator standing0/100
No investigator recorded in the registry for this trial

These describe the registry record only, and today we hold ClinicalTrials.gov data. Absent fields lower a score, and absence often reflects registration practice rather than study quality. A high-stature trial is not necessarily safer or a better choice for you — enrolling in a large definitive trial can mean a higher chance of receiving placebo, while a small early-phase study may be the only route to a new therapy.

תקציר

This is a prospective, single arm, multicenter study. Subjects with bicuspid aortic valve morphology will be enrolled in a separate registry.

מצבים רפואיים

Aortic Stenosis, Severe

זכאות

זכאות
מין	הכול
גילאים	לא צוין ברשומת המרשם
מתנדבים בריאים	לא

זכאות כפי שנכתבה במרשם

Inclusion Criteria: 1. Severe, calcific AS 2. Native aortic annulus size suitable for SAPIEN X4 THV 3. NYHA functional class ≥ II 4. The subject has been informed of the nature of the study, agrees to its provisions and has provided written informed consent. Exclusion Criteria: 1. Anatomical characteristics that would preclude safe femoral placement of the introducer sheath or safe passage of the delivery system 2. Aortic valve is unicuspid, bicuspid or non-calcified 3. Pre-existing mechanical or bioprosthetic valve in any position 4. Severe aortic regurgitation (\> 3+) 5. Severe mitral regurgitation (\> 3+) or ≥ moderate mitral stenosis 6. Need for mitral, tricuspid or pulmonic valve intervention within the next 12 months 7. Left ventricular ejection fraction \< 20% 8. Cardiac imaging evidence of intracardiac mass, thrombus or vegetation 9. Left ventricular outflow tract calcification that would increase the risk of annular rupture or significant PVL after THV implantation 10. Increased risk of coronary artery obstruction after THV implantation 11. Myocardial infarction within 30 days prior to the study procedure 12. Hypertrophic cardiomyopathy with subvalvular obstruction 13. Subjects with planned concomitant ablation for atrial fibrillation 14. Complex coronary artery disease (CAD) that cannot be optimally treated by percutaneous coronary intervention (PCI) 15. Any surgical or transcatheter procedure within 30 days prior to the study procedure (unless part of planned strategy for treatment of CAD). Implantation of a permanent pacemaker or implantable cardioverter defibrillator (ICD) is not considered an exclusion. 16. Any planned surgical or transcatheter intervention to be performed within 30 days following the study procedure (unless part of planned strategy for treatment of CAD) 17. Endocarditis within 180 days prior to the study procedure 18. Stroke, transient ischemic attack or neurological signs and symptoms attributed to carotid or vertebrobasilar disease within 90 days prior to the study procedure 19. Hemodynamic or respiratory instability requiring inotropic or mechanical support within 30 days prior to the study procedure 20. Renal insufficiency and/or renal replacement therapy 21. Leukopenia, anemia, thrombocytopenia 22. Inability to tolerate or condition precluding treatment with antithrombotic therapy 23. Hypercoagulable state or other condition that increases risk of thrombosis 24. Absolute contraindications or allergy to iodinated contrast that cannot be adequately treated with premedication 25. Subject refuses blood products 26. BMI \> 50 kg/m2 27. Estimated life expectancy \< 24 months 28. Female who is pregnant or lactating 29. Active SARS-CoV-2 infection or previously diagnosed with COVID-19 with sequelae that could confound endpoint assessments 30. Participating in another investigational drug or device study that has not reached its primary endpoint 31. Subject considered to be part of a vulnerable population

זכאות במשפטים פשוטים

הקריטריונים של רשומה זו טרם פורקו למשפטים נפרדים. טקסט המרשם שלמעלה שלם והוא הגרסה המחייבת.

תכנון המחקר

תכנון המחקר
סוג המחקר	התערבותי
שלב	לא רלוונטי
הקצאה	לא אקראי
מודל ההתערבות	SINGLE_GROUP
מטרה ראשית	TREATMENT
הסתרה	NONE (0)
גיוס	דרושים 1,234 משתתפים

נותן חסות ושותפים

Edwards Lifesciences נותן חסות

זרועות והתערבויות

TAVR - Main CohortEXPERIMENTAL
Subjects will undergo transcatheter aortic valve replacement (TAVR)
TAVR - Bicuspid RegistryEXPERIMENTAL
Subjects with bicuspid aortic valve morphology will undergo TAVR
TAVR - X4S RegistryEXPERIMENTAL
Subjects will undergo transcatheter aortic valve replacement (TAVR)

התערבויות

התקן SAPIEN X4 THV
Implantation of the SAPIEN X4 valve
התקן SAPIEN X4S
Implantation of the SAPIEN X4S valve

מדדי תוצאה

מדד תוצאה ראשוני
Non-hierarchical composite of death and stroke
The number of patients that died or had a stroke
מסגרת זמן 1 year
מדד תוצאה משני
Favorable outcome per VARC-3: Composite of 1) alive, 2) Kansas City Cardiomyopathy Questionnaire (KCCQ) score ≥ 60, and 3) KCCQ score decrease ≤10 points from baseline
The number of patients that met all of these criteria. The KCCQ is a 23-item, self-administered instrument that quantifies physical function, symptoms (frequency, severity and recent change), social function, self-efficacy and knowledge, and quality of life. An overall summary score can be derived from the physical function, symptom (frequency and severity), social function and quality of life domains. Scores are transformed to a range of 0-100, in which higher scores reflect better health status.
מסגרת זמן 1 year
מדד תוצאה משני
Paravalvular leak
Paravalvular leak will be categorized as None, Trace, Mild, Mild-Moderate, Moderate, Moderate-Severe, or Severe
מסגרת זמן 30 days
מדד תוצאה משני
New permanent pacemaker implantation
The number of patients with this event
מסגרת זמן 30 days

תאריכים

תאריכים
תאריך התחלה	20 ביוני 2022 (בפועל)
סיום ראשוני	1 ביולי 2027 (משוער)
סיום	1 בינואר 2037 (משוער)
פורסם לראשונה	29 בדצמבר 2021 (בפועל)
עודכן לאחרונה	3 בספטמבר 2026
התוצאות פורסמו	לא צוין ברשומת המרשם
המצב אומת לאחרונה	אוגוסט 2026

בפועל פירושו שהאירוע התרחש. משוער פירושו שנותן החסות צופה אותו. שתי המשמעויות שונות זו מזו.

מיקומים

26 אתרים מגייסים

Australia

Australia
מתקן	עיר	מדינה או אזור	מצב
Royal Adelaide Hospital	Adelaide	South Australia	פעיל, ללא גיוס
The Royal Melbourne Hospital	Parkville		פעיל, ללא גיוס
St. Andrews War Memorial Hospital	Spring Hill	Queensland	פעיל, ללא גיוס

Canada

Canada
מתקן	עיר	מדינה או אזור	מצב
Hamilton Health Services	Hamilton	Ontario	פעיל, ללא גיוס
Institut Universitaire de Cardiologie et de Pneumologie de Quebec- Universite Laval	Québec	Quebec	פעיל, ללא גיוס
St. Paul's Hospital System	Vancouver	British Columbia	פעיל, ללא גיוס

New Zealand

New Zealand
מתקן	עיר	מדינה או אזור	מצב
Christchurch Hospital	Christchurch		פעיל, ללא גיוס

United States

United States
מתקן	עיר	מדינה או אזור	מצב
Piedmont Heart Institute	Atlanta	Georgia	פעיל, ללא גיוס
Emory University Atlanta	Atlanta	Georgia	פעיל, ללא גיוס
Medstar Union Memorial Hospital	Baltimore	Maryland	מגייס
Brigham and Women's Hospital	Boston	Massachusetts	מגייס
University at Buffalo - Kaleida Health	Buffalo	New York	מגייס
St. Vincent Medical Group, Inc./ St. Vincent Heart Center of Indiana, LLC	Carmel	Indiana	פעיל, ללא גיוס
Carolinas Health System	Charlotte	North Carolina	פעיל, ללא גיוס
Novant Health and Heart Vascular Institute	Charlotte	North Carolina	מגייס
Rush University Medical Center Chicago	Chicago	Illinois	פעיל, ללא גיוס
The Christ Hospital	Cincinnati	Ohio	מגייס
Kaiser Portland	Clackamas	Oregon	מגייס
The Cleveland Clinic Foundation	Cleveland	Ohio	פעיל, ללא גיוס
Medical City Dallas Hospital	Dallas	Texas	פעיל, ללא גיוס
Baylor Heart and Vascular Hospital	Dallas	Texas	מגייס
Henry Ford Hospital	Detroit	Michigan	פעיל, ללא גיוס
Alexian Brothers Hospital Network	Elk Grove Village	Illinois	מגייס
NorthShore University HealthSystem Research Institute Evanston	Evanston	Illinois	מגייס
Northwestern University Chicago	Evanston	Illinois	מגייס
Methodist Le Bonheur Healthcare	Germantown	Tennessee	פעיל, ללא גיוס
Pinnacle Health Harrisburg	Harrisburg	Pennsylvania	הושלם
Hartford Hospital	Hartford	Connecticut	פעיל, ללא גיוס
HCA Houston Healthcare Medical Center	Houston	Texas	פעיל, ללא גיוס
University of Texas Memorial Hermann	Houston	Texas	פעיל, ללא גיוס
University of Kansas Medical Center	Kansas City	Kansas	פעיל, ללא גיוס
Saint Luke's Hospital	Kansas City	Missouri	פעיל, ללא גיוס
Scripps Memorial Hospital La Jolla	La Jolla	California	פעיל, ללא גיוס
Dartmouth-Hitchcock Medical Center, Hanover	Lebanon	New Hampshire	מגייס
Kaiser Los Angeles	Los Angeles	California	פעיל, ללא גיוס
Cedars-Sinai Medical Center	Los Angeles	California	מגייס
UC Health Northern Colorado (Medical Center of the Rockies)	Loveland	Colorado	פעיל, ללא גיוס
St. Patrick Hospital	Missoula	Montana	פעיל, ללא גיוס
Atlantic Health System Morristown	Morristown	New Jersey	מגייס
Centennial Medical Center	Nashville	Tennessee	מגייס
Saint Thomas Health	Nashville	Tennessee	מגייס
Vanderbilt University Medical Center	Nashville	Tennessee	מגייס
Rutgers Robert Wood Johnson Medical School	New Brunswick	New Jersey	מגייס
Silver Cross Hospital	New Lenox	Illinois	מגייס
Columbia University Medical Center/NYPH	New York	New York	מגייס
Cornell Medical Center	New York	New York	מגייס
Montefiore Medical Center	New York	New York	פעיל, ללא גיוס
Hoag Memorial Hospital Presbyterian	Newport Beach	California	פעיל, ללא גיוס
Sentara Norfolk General Hospital	Norfolk	Virginia	פעיל, ללא גיוס
Naples Community Hospital Healthcare System	North Naples	Florida	פעיל, ללא גיוס

15 אתרים נוספים מצוינים ברשומת המרשם.

מסמכי המחקר

לא צורפו מסמכים ברשומת מרשם זו.

שינויים לאורך זמן

לא נרשמו שינויים מאז שקלטנו רשומה זו לראשונה.

שינוי נרשם בכל פעם שנותן החסות מעדכן את רשומת המרשם. מצב, תאריכים, גיוס ואתרים מופיעים כאן ככל שהם משתנים.

מרשם: ClinicalTrials.gov · NCT########

https://xmedica.io/trials/ctgov/NCT05172960