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Venus Panorama II Post-marketing Registry Study

Venus Panorama II Post-marketing Registry Study

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2200059960
Enrollment
Unknown
Registered
2022-05-14
Start date
2022-05-02
Completion date
Unknown
Last updated
2024-04-15

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

Conditions

None listed

Interventions

Case series:Venus TAVR System

Sponsors

Qilu Hospital, Shandong University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1.Patients who have received or will receive Venus TAVR System to treat aortic valve disease; 2.Willing to sign the ICF of the study and complete the follow-up according to the study requirements.

Exclusion criteria

Exclusion criteria: 1. Not willing to sign the informed consent form; 2. Unable to comply with the study protocol and complete clinical follow-up for various reasons; 3. The investigator evaluated that the patient was not suitable for transcatheter aortic valve replacement.

Design outcomes

Primary

MeasureTime frame
All cause mortality;Function of bioprosthetic valves;

Countries

China

Contacts

Public ContactFangni Wang

Venus Medtech (Hangzhou) Inc.

wangfangni@venusmedtech.com+86 15910739862

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026