EASE TRICUSPID Expertise-based Assessment Study on Clinical Efficacy of Contour 3D® in TRICUSPID Valve Annuloplasty

Completed

Conditions: Tricuspid Valve Insufficiency

Interventions: Procedure: Tricuspid valve repair
Procedure: Left-sided heart surgery
Device: Contour 3D Tricuspid Annuloplasty Ring

Registration Number: NCT01532921

Lead Sponsor: Medtronic Bakken Research Center

Brief Summary: Few clinical evidence for the Contour 3D Tricuspid Annuloplasty Ring exists; therefore, in order to position this product on the market, a post-market release study was completed. The purpose of this study was to evaluate the hemodynamic performance of the Contour 3D® Tricuspid Annuloplasty Ring following Tricuspid Valve (TV) repair in a post-market environment.

Detailed Description: The EASE TRICUSPID Clinical Trial was a prospective, non-randomized, non-interventional, post-market release study. The purpose of this study was to evaluate the hemodynamic performance of the Contour 3D® Tricuspid Annuloplasty Ring following Tricuspid Valve (TV) repair in a post-market environment. Therefore, the primary objective of the EASE Tricuspid Study was to evaluate the hemodynamic performance of the Contour 3D® Tricuspid Annuloplasty Ring (Contour 3D ring) in subjects with tricuspid regurgitation who had a clinical indication for TV repair in a post-market use. Secondary objectives included the evaluation of the effect of TV repair with the Contour 3D ring on the right ventricular function, as well as the assessment of the effect of TV repair with the Contour 3D ring on the functional status in subjects undergoing TV repair in a post-market environment. Subjects eligible for TV repair and compliant with the enrollment criteria were considered by the Investigator for inclusion in the study. To minimize bias, enrolled subjects were followed by their own physician in accordance with the center's established practice for routine follow up. Follow-up sessions were planned at the physician's discretion. To meet the intended goals, appropriate clinical data were collected at baseline (pre-surgery), during the surgical procedure, at discharge and during the follow-up period at 6 months. Experienced echo-cardiologists evaluated the echos. At the time of enrollment it was not certain if the subject would receive a Contour 3D ring, since the surgeon might have decided during surgery that another treatment was more beneficial to the subject. In this case, the subject was terminated from the study.

Recruitment & Eligibility

Status: COMPLETED

Sex: All

Target Recruitment: 85

Inclusion Criteria

Willing to sign and date the Patient Informed Consent (PIC)
Indicated for a concomitant surgical repair of the TV
Willing to return to the hospital, where the implantation originally occurred, for a 6 month follow-up visit

Exclusion Criteria

Patients with a degenerative TV condition
Patients with primary TV regurgitation
Previous TV repair or replacement
Stand-alone TV repair
Already participating in another investigational device or drug study, possibly leading to bias and jeopardizing the scientific appropriate assessment of the study endpoints
Life expectancy of less than one year
Pregnant or desire to be pregnant within 12 months of the study treatment
Under 18 years or over 85 years of age
Patients with active endocarditis
Patients with valvular retraction with severely reduced mobility
Patients with a heavily calcified TV

Study & Design

Study Type: OBSERVATIONAL

Study Design: Not specified

Arm && Interventions

Group	Intervention	Description
Subjects with Tricuspid Valve Repair	Contour 3D Tricuspid Annuloplasty Ring	All patients indicated for a Tricuspid Valve (TV) repair procedure concomitantly to left-sided heart surgery, and for whom the surgeon considers the implantation of a Contour 3D® Tricuspid Annuloplasty Ring most appropriate to reconstruct the diseased valve.
Subjects with Tricuspid Valve Repair	Tricuspid valve repair	All patients indicated for a Tricuspid Valve (TV) repair procedure concomitantly to left-sided heart surgery, and for whom the surgeon considers the implantation of a Contour 3D® Tricuspid Annuloplasty Ring most appropriate to reconstruct the diseased valve.
Subjects with Tricuspid Valve Repair	Left-sided heart surgery	All patients indicated for a Tricuspid Valve (TV) repair procedure concomitantly to left-sided heart surgery, and for whom the surgeon considers the implantation of a Contour 3D® Tricuspid Annuloplasty Ring most appropriate to reconstruct the diseased valve.

Primary Outcome Measures

Name	Time	Method
Change in Tricuspid Valve (TV) Leaflet Coaptation Length From Baseline Through 6 Months Post-implant	Baseline to Discharge (up to 5 days post-implant) and to 6 months post-implant	Change in the degree of TV leaflet coaptation length measured via echocardiography from Baseline through 6 months post-implant
Change in the Degree of Tricuspid Valve (TV) Leaflet Tethering Height From Baseline Through 6 Months Post-implant	Baseline to Discharge (up to 5 days post-implant) and 6 months post-implant	Change in the degree of TV leaflet tethering height measured via echocardiography from Baseline through 6 months post-implant
Mean Gradient Across the Tricuspid Valve	At Baseline, Discharge (up to 5 days post-implant) and 6 months post-implant	The mean gradient across the Tricuspid Valve (TV) measured via echocardiography at discharge (up to 5 days post-implant) through 6 months post-implant
Change in the Degree of Tricuspid Regurgitation From Baseline Through Discharge (up to 5 Days Post-implant) and 6 Months Post-implant	Baseline to Discharge (up to 5 days post-implant) and through 6 months post-implant	Change in the degree of tricuspid regurgitation measured via echocardiography from Baseline through 6 months post-implant. The severity of tricuspid regurgitation is graded by using several qualitative and quantitative methods. The degree of regurgitation is classified as "none", "Mild", "Moderate" or "Severe".

Secondary Outcome Measures

Name	Time	Method
Change in the Right Ventricle (RV) Diastolic Area From Baseline Through 6 Months Post-implant	Basline to Discharge (up to 5 days post-implant) and 6 months post-implant
Change in the Tricuspid Annular Diameter Measured at Diastole From Baseline Through 6 Months Post-implant	Baseline to Discharge (up to 5 days post-implant) and 6 months post-implant
Change in the Right Ventricle (RV) Fractional Area From Baseline Through 6 Months Post-implant	Baseline to Discharge (up to 5 days post-implant) and 6 months post-implant
Change in New York Heart Association (NYHA) Classification From Baseline Through 6 Months Post-implant	Baseline to Discharge (up to 5 days post-implant) and 6 months post-implant	The New York Heart Association (NYHA) Functional Classification provides a simple way of classifying the extent of heart failure. It places patients in one of four categories based on how much they are limited during physical activity; the limitations/symptoms are in regard to normal breathing and varying degrees in shortness of breath and/or angina. NYHA I implies no limitations. NYHA II implies slight limitation of physical activity. NYHA III implies marked limitation of physical activity and finally, NYHA IV implies patients are Unable to carry on any physical activity without discomfort.

Trial Locations

Locations (7): Shaare Zedek Medical Center
🇮🇱
Jerusalem, Israel
Hôpital de Lyon - Hôpital Louis Pradel
🇫🇷
Lyon, France
Albertinen Herz- und Gefäßzentrum
🇩🇪
Hamburg, Germany
Universitätsklinikum Schleswig-Holstein
🇩🇪
Lübeck, Germany
Centre Hospitalier de Mulhouse
🇫🇷
Mulhouse, France
Deutsches Herzzentrum München
🇩🇪
Munich, Germany
Soroka Medical Center
🇮🇱
Be'er Sheeva, Israel