Clinical Study to Evaluate the Performance of Perimount Heart Valve in Chinese Patients

Edwards Lifesciences

Status: Completed

Conditions: Mitral Valve or Aortic Valve Replacement

Study type: Observational

Funder types: Industry

Identifiers

NCT02400489

Perimount CN001

Details and patient eligibility

About

To recruit patients who implanted with Perimount Heart Valve (Type Number: 6900PTFX or 2800TFX) from three hospitals in China.

To track the patients'situations during one year after surgery and to collect the relevant clinical data.

Enrollment: 265 patients

Sex: All

Volunteers: No Healthy Volunteers

Inclusion criteria

• Patients implanted with Perimount 6900PTFX after 2012-11-19 or with Perimount 2800TFX after 2013-8-20
• Patients sign the Inform Consent Form (ICF) and agree to join the study

Exclusion criteria

• Don't have any specific exclusion criteria.