Band Versus Ring for Tricuspid Regurgitation

Not Applicable

• Conditions: Tricuspid Regurgitation
• Interventions: Procedure: Tricuspid Annuloplasty

• Registration Number: NCT04093297
• Lead Sponsor: Nanjing Medical University

Brief Summary

Tricuspid regurgitation is common in patients with heart valve disease, both flexible band and rigid ring annuloplasty can correct this anomaly. However, there is no data to address which one can bring more benefits to these patients with combined heart valve disease. This study aims to prospectively compare the efficacy and long term outcomes of flexible band versus rigid ring annuloplasty for the correction of tricuspid regurgitation.

Detailed Description

Not available

Study Timeline

• Study First Submitted: 2019-09-16
• Study First Submitted QC: 2019-09-16
• Study First Posted: 2019-09-18
• Study Start: 2021-01-01
• Status Verified: 2022-04
• Last Update Submitted: 2022-04-06
• Last Update Posted: 2022-04-14
• Primary Completion: 2022-12
• Study Completion: 2022-12

Recruitment & Eligibility

• Status: UNKNOWN
• Sex: All
• Target Recruitment: 300

Inclusion Criteria

• 1. Subject must be 18 years and 80 years at time of consent and must not be a member of a vulnerable population.
• 2. Subject or a legally authorized representative (where allowed per local regulations) must provide written informed consent prior to any trial related procedure.
• 3. Subjects with moderate or greater tricuspid regurgitation determined by the assessment of a qualifying transthoracic echocardiogram (TTE) and/or transesophageal echocardiogram (TEE).
• 4. Subjects with moderate tricuspid regurgitation will only be included in the trial if moderate tricuspid regurgitation is accompanied by a tricuspid annular diameter of ≥ 40mm as measured by echocardiography.
• 5. Isolated functional symptomatic tricuspid regurgitation of moderate to severe or greater, with annular dilatation of ≥ 40mm;
• 6. Requirement for concomitant left heart valve surgery;
• 7. Requirement for concomitant coronary artery surgery;
• 8. Requirement for concomitant atrial fibrillation surgery;
• 9. Available and able to return to the study site for post-procedural follow-up examination;

Exclusion Criteria

• 1. Patient unable or unwilling to provide informed consent;
• 2. Subjects with mild tricuspid regurgitation;
• 3. Emergency surgery;
• 4. Prior tricuspid valve leaflet surgery or any currently implanted prosthetic tricuspid valve, or any prior transcatheter tricuspid valve procedure;
• 5. Subjects with percutaneous coronary intervention within prior 30 days prior to enrollment;
• 6. Subjects with presence of any known life threatening (non-cardiac major or progressive disease), non-cardiac disease that will limit the subject's life expectancy to less than one year;
• 7. Subjects with permanent or temporary pacemaker implantation;
• 8. Subjects with severe, irreversible pulmonary hypertension in the judgment of the investigator;
• 9. History of mitral/tricuspid endocarditis within the last 12 months;
• 10. Subjects with contraindication or known allergy to device's components, aspirin, anti-coagulation therapy or contrast media that cannot be adequately premeditated;
• 11. Subjects with bleeding or coagulation disorders (e.g. active peptic ulcer or active gastrointestinal bleeding);
• 12. Female patient is pregnant (urine HCG test result positive) or lactating;
• 13. Subject is currently participating in another clinical trial that has not yet completed its primary endpoint;
• 14. Subjects with left ventricular ejection fraction (LVEF)≤20%.

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Group Band	Tricuspid Annuloplasty	Patients in Group Band will undergo flexible band annuloplasty
Group Ring	Tricuspid Annuloplasty	Patients in Group Ring will undergo tricuspid rigid ring annuloplasty

Primary Outcome Measures

Name	Time	Method
Improvement in severity of tricuspid regurgitation	within 3 months	Improvement in tricuspid regurgitation: refers to Mild or No tricuspid regurgitation Tricuspid regurgitation is graded as mild, moderate, and severe based on regurgitant jet area

Secondary Outcome Measures

Name	Time	Method
Mortality	up to 3 months of intervention	Mortality: Mortality within hospital stay or 1 month postoperative.

Trial Locations

Locations (1)

The First Affiliated Hospital of Nanjing Medical University; 🇨🇳 Nanjing, China