Actively Recruiting
Comparison of Transcatheter Edge-to-edge Repair Using Echo Only with Echo Combined with X Ray for Mitral Regurgitation (ECHO-CLIP)
Led by Pan Xiangbin · Updated on 2024-11-12
200
Participants Needed
1
Research Sites
135 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Mitral regurgitation (MR) is a common valvular heart disease in the elderly population, frequently associated with poor prognosis if not treated. Transcatheter edge-to-edge repair (TEER) has recently emerged as a popular strategy due to minimal invasiveness. What's more, previous studies, such as EVEREST II and COAPT study, have demonstrated its efficacy in high-risk patients with primary or secondary MR. Conventional TEER procedure, however, is performed under combined guidance of both echocardiography and fluoroscopy, which potentially results in high radiation exposure and limits its application. Since 2021 2021, the investigators have changed the procedural methodology by performing TEER under full echocardiographic guidance on accumulated dozens of MR patients successfully. To confirm the efficacy of a fully echo-guided TEER procedure, the investigators conduct the ECHO-CLIP study to compare its outcomes with the conventional TEER procedure, as well as evaluate the outcomes of this novel methodology in special populations with radiation contraindications. ECHO-CLIP study is a prospective, multicenter, open-label, noninferior, randomized controlled trial of TEER by two different methodological strategies in treating severe primary or secondary MR. It is anticipated to enroll a total of 200 patients as well to complete the enrollment before Dec 31, 2025 and the follow-up before Dec 31, 2026. This work will potentially demonstrate the feasibility and efficacy of the fully echo-guided TEER procedure, thereby revolutionizing the TEER methodology and benefiting more patients.
CONDITIONS
Official Title
Comparison of Transcatheter Edge-to-edge Repair Using Echo Only with Echo Combined with X Ray for Mitral Regurgitation (ECHO-CLIP)
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Symptomatic degenerative mitral regurgitation (DMR) with MR severity of 3+ or higher and high surgical risk defined by STS Predicted Risk of Mortality replacement score of 8 or higher or repair score of 6 or higher
- Functional mitral regurgitation (FMR) with left ventricular end-systolic diameter (LVESD) of 70 mm or less and MR severity of 3+ or higher despite 30 days of guideline-directed medical therapy (GDMT)
- Mitral valve (MV) anatomy suitable for transcatheter edge-to-edge repair (TEER)
- Willingness to participate and complete scheduled follow-up after informed consent
You will not qualify if you...
- Myocardial infarction within 12 weeks before randomization
- Need for other concurrent cardiac procedures
- Any endovascular intervention or surgery within 30 days before randomization
- Left ventricular ejection fraction (LVEF) less than 20%
- Mitral valve orifice area less than 4.0 cm²
- Pulmonary artery systolic pressure greater than 70 mmHg
- Severe mitral annular calcification
- Mitral valve anatomy unsuitable for clip implantation due to leaflet calcification or cleft in grasping zone
- Previous mitral valve surgery, or current ventricular assist device or mechanical prosthetic valve
- Presence of intracardiac mass, thrombus, or vegetation
- Active endocarditis or rheumatic heart disease
- History of deep venous thrombosis (DVT) or pulmonary embolism (PE)
AI-Screening
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Trial Site Locations
Total: 1 location
1
Fuwai Hospital Chinese Academy of Medical Sciences Shenzhen
Shenzhen, Guangdong, China, 518000
Actively Recruiting
Research Team
X
Xiangbin Pan
CONTACT
J
Jianrui Ma
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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