RCT of Minimalist vs Standard Procedure for LAAC in NVAF Patients

Not Applicable

Not yet recruiting

• Conditions: Atrial Fibrillation; Left Atrial Appendage Occlusion; General Anesthesia; Local Anesthesia

• Registration Number: NCT06969118
• Lead Sponsor: Shanghai Zhongshan Hospital

Brief Summary

Percutaneous left atrial appendage closure (LAAC) is an effective strategy for stroke prevention in patients with non-valvular atrial fibrillation (NVAF). Standard procedure requires general anesthesia, transesophageal echocardiography (TEE) guidance. With the experience accumulation, LAAC can be successfully completed in many centers under local anesthesia, the guidance of X-ray and transthoracic echocardiography (TTE), also known as minimalist procedure. Our center was one of the earliest to carry out minimalist procedure worldwide. At present, expert consensus suggests that minimalist procedure is feasible in experienced centers, but the relevant evidence is insufficient. Some single-arm studies have shown that minimalist procedure is safe and effective. However, there is currently a lack of direct evidence to compare the strengths and weaknesses of these two LAAC procedures. The goal of the study was to compare the effectiveness and safety of minimalist procedure and standard procedure for LAAC in patients with NVAF.

Detailed Description

This is a prospective, randomized, controlled, multi-center clinical study designed to compare the safety and efficacy of minimalism transcatheter LAAC versus standard transcatheter LAAC in NVAF patients. The study aims to enroll approximately 200 NVAF patients requiring transcatheter LAAC at 20 to 30 research centers in China. All eligible patients who sign the informed consent form will be randomly assigned to either the minimalism transcatheter LAAC group or the standard transcatheter LAAC group in a 1:1 ratio. The study will record preoperative baseline information and follow-up data at 7 days post-Procedure or discharge, and at 2, 6, and 12 months post-Procedure, to explore the incidence of procedure-related complications and peridevice leak ≤5mm between the two groups.

Study Timeline

• Study First Submitted: 2024-08-30
• Status Verified: 2025-05
• Study First Submitted QC: 2025-05-06
• Last Update Submitted: 2025-05-06
• Study First Posted: 2025-05-13
• Last Update Posted: 2025-05-13
• Study Start: 2025-06-01
• Primary Completion: 2027-06-01
• Study Completion: 2027-06-01

Recruitment & Eligibility

• Status: NOT_YET_RECRUITING
• Sex: All
• Target Recruitment: 200

Inclusion Criteria

1. Age 18 - 85 years old, all genders;
2. Subjects who can understand the purpose of the trial, participate voluntarily and sign the informed consent form, and are willing to complete the follow-up according to the protocol requirements;
3. Indications for left atrial appendage closure: non-valvular atrial fibrillation patients with CHA2DS2-VAS2 score ≥2 and HAS-BLED score ≥3, or who are unable or unwilling to receive long-term oral anticoagulants;
4. Life expectancy ≥1 year;

Exclusion Criteria

1. Preoperative TEE/heart CT/intracardiac ultrasound suggested thrombus in the left atrial appendage/left atrium;
2. Patients with severe renal insufficiency (creatinine ≥200 μmol/L, creatinine clearance <30 ml/min);
3. Liver disease patients with coagulation abnormalities and clinically relevant bleeding risks, including liver cirrhosis patients reaching Child Pugh stages B and C;
4. Severely decreased platelet count at baseline: PLT ≤50*10^9/L;
5. Patients with severe preoperative cardiac insufficiency (LVEF <35%; clinical manifestations are uncontrolled class IV heart failure);
6. Combined with other severe cardiac valvular diseases or other structural abnormalities that require surgical treatment on an elective day; or severe coronary heart disease that requires intervention within a fixed period;
7. Patients who have lesions or conditions with a significant risk of major bleeding, such as current or recent gastrointestinal ulcers, malignant tumors with a high risk of bleeding, recent brain or spinal injuries, recent brain, spinal or ophthalmic procedure, recent intracranial hemorrhage, known or suspected esophageal varices, arteriovenous malformations, vascular aneurysms, or major intraspinal or intracerebral vascular malformations;
8. Patients with concurrent diseases (other than atrial fibrillation) that require anticoagulant therapy (such as after mechanical valve replacement, and spontaneous or recurrent venous thromboembolism);
9. Patients who are in clinical trials of other drugs or medical devices and have not completed it yet;
10. Patients who are considered ineligible to participate in the clinical trial by the investigator.

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Primary Outcome Measures

Name	Time	Method
primary safety	7 days after LAAC procedure	Occurrence of a composite endpoint about serious perioperative complications including all-cause death, ischemic or hemorrhagic stroke, systemic embolism, and procedure related complications requiring thoracotomy or endovascular intervention treatment.
primary efficacy	From LAAC procedure to the end of treatment at 12 months	Occurrence of successful device implantation under predetermined guidance as well as effective LAA closure with residual leak ≤ 5mm

Secondary Outcome Measures

Name	Time	Method
the amount of radiation	Perioperation	the amount of intraoperative radiation (Gy)
hospitalization time	Perioperation	hospitalization time (days)
The number of replacements of the device.	Perioperation	The number of replacements of the device.
All procedure-related complications	at 2, 6, and 12 months post-procedure	Occurrence of all procedure-related complications
Effective LAA closure	at 2, 6, and 12 months post-procedure	The occurrence rate of effective LAA closure (residual leak ≤5mm)
Bleeding events;	at 2, 6, and 12 months post-procedure	Occurrence of bleeding events
All-cause death;	at 2, 6, and 12 months post-procedure	Occurrence of all-cause death
Cardiac death;	at 2, 6, and 12 months post-procedure	Occurrence of cardiac death
Device-related thrombosis events;	at 2, 6, and 12 months post-procedure	Occurrence of device-related thrombosis events
Immediate procedure success rate	Perioperation	The occurrence rate of successful device implantation under predetermined guidance
The duration of the procedure	Perioperation	The duration of the LAAC procedure (minutes)
the amount of contrast medium	Perioperation	the amount of intraoperative contrast medium (ml)
Stroke/transient ischemic attack and systemic embolism	at 2, 6, and 12 months post-procedure	Occurrence of stroke/transient ischemic attack and systemic embolism

Trial Locations

Locations (1)

Zhongshan Hospital,Fudan Univerisity; 🇨🇳 Shanghai, Shanghai, China