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Echocardiography Guided TAVR (Echo TAVR)

Transcatheter Aortic Valve Replacement With Echocardiography Guidance

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07030062
Enrollment
20
Registered
2025-06-19
Start date
2025-02-18
Completion date
2025-12-31
Last updated
2025-06-19

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Echocardiography, Transcatheter Aortic Valve Replacemen

Brief summary

Conventional transcatheter aortic valve replacement (TAVR) relies on fluoroscopic and contrast agents. However, in high-risk patients, exposure to ionizing radiation and contrast agents is contraindicated and undesirable. Echocardiography guidance TAVR can offer a feasible and safer strategy for TAVR.

Interventions

None listed

Sponsors

Pan Xiangbin
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

1. symptomatic severe AS determined by echocardiography and Doppler that requiring aortic valve replacement, which is defined as: mean gradient ≥40 mmHg, peak aortic velocity ≥4 m/s, and aortic valve area (AVA) ≤1 cm2 (or an indexed AVA ≤0.6 cm2/m2); 2. a history of malignancy or a high familial risk of cancer, with refusal to undergo contrast- or radiation-guided procedures; 3. chronic kidney disease and refuse to receive contrast agents or radiation exposure.

Exclusion criteria

Required hybrid procedures or concomitant interventions on other cardiac malformations; Deemed inoperable due to extremely high surgical risk or severe comorbidities; Had untreated clinically significant coronary vascular disease amenable to revascularization; Previously undergone aortic valve replacement.

Design outcomes

Primary

MeasureTime frameDescription
Valve Academic Research Consortium-3 (VARC-3)30-day after surgeryVARC3 include but not limited to Mortality (all-cause and cardiovascular) Stroke and transient ischemic attack (TIA) Acute kidney injury Conduction disturbances and permanent pacemaker implantation Bleeding (updated using BARC criteria) Myocardial infarction Vascular access complications Endocarditis

Countries

China

Contacts

Primary ContactXiangbin Pan, MD
panxiangbin@fuwaihospital.org88396655
Backup ContactFengwen Zhang, MD
88396654

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026