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Active, not recruiting Not applicable Interventional

The JenaValve ALIGN-AR LVAD Registry

ClinicalTrials.gov ID: NCT06594705

Public ClinicalTrials.gov record NCT06594705. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Sep 5, 2026, 7:30 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

Transcatheter Aortic Valve Replacement Using the JenaValve TrilogyTM Heart Valve System for Clinically Significant Aortic Regurgitation in Patients With Left Ventricular Assist Devices (LVAD)

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

To evaluate the safety and effectiveness of the JenaValve Trilogy™ Heart Valve System for transcatheter aortic valve replacement (TAVR) in subjects with continuous flow left ventricular assist devices (cfLVAD) and clinically significant aortic regurgitation (AR) who are indicated for TAVR

Study identification

NCT ID
NCT06594705
Recruitment status
Active, not recruiting
Study type
Interventional
Phase
Not applicable
Lead sponsor
JenaValve Technology, Inc.
Industry
Enrollment
50 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Dec 8, 2024
Primary completion
Jul 31, 2026
Completion
Jul 31, 2027
Last update posted
Jul 21, 2026

2024 – 2027

United States locations

U.S. sites
14
U.S. states
11
U.S. cities
14
Facility City State ZIP Site status
Cedars-Sinai Medical Center Los Angeles California 90048
Sutter Health San Francisco California 94109
Medstar Washington Hospital Center Washington D.C. District of Columbia 20010
Piedmont Atlanta Georgia 30309
Advocate Christ Medical Center Oak Lawn Illinois 60453
University of Michigan Ann Arbor Michigan 48109
Henry Ford Hospital Detroit Michigan 48202
Minneapolis Heart Institute Foundation Minneapolis Minnesota 55407
Washington University, St. Louis St Louis Missouri 63130
Columbia University Medical Center/New York-Presbyterian Hospital New York New York 10032
Houston Methodist Research Center Houston Texas 77030
Baylor Plano Texas 75024
Intermountain Murray Utah 84107
Sentara Norfolk General Hospital Norfolk Virginia 23507

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT06594705, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Jul 21, 2026 · Synced Sep 5, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT06594705 live on ClinicalTrials.gov.

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