Comparison Between Upgraded '2C3L' vs. PVI Approach for Catheter Ablation of Persistent Atrial Fibrillation

Persistent Atrial Fibrillation Clinical Trial

— PROMPT-AF  

Official title:

Prospective Randomized Comparison Between Upgraded '2C3L' vs. PVI Approach for Catheter Ablation of Persistent Atrial Fibrillation

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT04497376
• Other study ID #: 2017YFC0908803
• Status: Recruiting
• Phase: N/A
• Start date: August 27, 2021
• Est. completion date: June 2024

Study information

• Verified date: August 2023
• Source: Beijing Anzhen Hospital
• Contact: Du Xin, Doctor
• Phone: 86-10-64420102
• Email: duxinheart[@]sina.com
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Catheter ablation has emerged as an important treatment option for patients with symptomatic atrial fibrillation (AF). Pulmonary vein antral isolation (PVI) is now considered the cornerstone technique of AF ablation and has shown promise in treating paroxysmal atrial fibrillation (PAF). However, there is no unique strategy for ablation of persistent AF (PeAF), whether PVI alone is sufficient to prevent patients from recurrence remains controversial. The PROMPT-AF study is a prospective, multicenter, randomized trial involving a blinded assessment of outcomes, which is designed to compare arrhythmia-free survival between PVI and an ablation strategy termed upgraded '2C3L' for ablation of PeAF.

Description:

The PROMPT-AF study will include 498 patients undergoing their first catheter ablation of PeAF. All patients will be randomized to either the upgraded '2C3L' arm or PVI arm in a 1:1 fashion. The upgraded '2C3L' technique is a fixed ablation approach consisting of EI-VOM, bilateral circumferential PVI, and three linear ablation lesion sets across the mitral isthmus, left atrial roof, and cavotricuspid isthmus. The follow-up duration is 12 months. The primary endpoint is the rate of documented atrial tachycardia arrhythmias of >30 seconds, without any antiarrhythmic drugs, in 12 months after the index ablation procedure (excluding a blanking period of 3 months).

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 498
• Est. completion date: June 2024
• Est. primary completion date: June 2024
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 80 Years

Eligibility

Inclusion criteria

Patients must meet all the following criteria to be included in the study:

1. age between 18 and 80,

2. patients undergoing a first-time ablation procedure for non-valvular AF,

3. patients with defined as a sustained episode more than 3 months

4. PeAF documented by ECG, Holter, loop recorder, telemetry, trans-telephonic monitor or implanted device within 90 days6 months of the ablation procedure,

5. patients experienced symptoms caused by AF and these symptoms include but are not limited to palpitations, presyncope, syncope, fatigue, and shortness of breath,

6. AF refractory to at least one AAD,

7. willingness, ability and commitment to provide informed consent and participate in follow-up evaluations.

Exclusion criteria Patients are to be excluded if any of the following criteria is met:

1. patients with paroxysmal AF,

2. patients with AF secondary to an obvious reversible cause,

3. patients with left atrial diameter = 60 mm in the parasternal long axis view,

4. left ventricular ejection fraction (LVEF) < 30%,

5. patients with triple (aspirin, clopidogrel and OAC) or dual (clopidogrel and OAC) antithrombotic therapy which predispose patients to higher risk of periprocedural bleeding. (e.g., Coronary percutaneous transluminal coronary angioplasty (PTCA)/stenting within the previous 90 days),

6. patients with contraindication to anticoagulation,

7. patients with contraindication to right or left sided heart catheterization,

8. pregnancy,

9. life expectancy less than 1 year (advanced malignant tumor, end stage renal disease, etc.),

10. patients cannot be removed from antiarrhythmic drugs for reasons other than AF.

Related Conditions & MeSH terms

• Atrial Fibrillation
• Catheter Ablation
• Persistent Atrial Fibrillation

Intervention

Procedure:
• upgraded '2C3L'
Patients randomized to the upgraded '2C3L' arm will first undergo EI-VOM, followed by the '2C3L' ablation step. The details include: (1). EI-VOM procedure: An 8.5-French-long sheath or a steerable long sheath is sent to the coronary sinus (CS) via the femoral vein. A JR4.0 catheter is inserted into the CS to identify the ostium of the VOM. Subsequently, a BMW wire supported by an OTW balloon catheter is advanced into the VOM. The balloon is inflated with 6 to 8 atm in the VOM. A selective venogram of the VOM is obtained by slowly injecting 1 mL of contrast medium. Then, ethanol is slowly injected into the VOM and selective venography of the VOM is repeated. (2) . After EI-VOM, radiofrequency ablation was performed to achieve bilateral pulmonary vein isolation and bidirectional block of mitral isthmus line, roof line, and cavotricuspid isthmus line. (3). Any organized AT observed during the procedure will be targeted as well.
• pulmonary vein antral isolation
After reconstructing the left atrial geometry, PVI will be performed (the right PV antrum (PVA) will be ablated first, followed by the left PVA. ) in a wide area circumferential pattern. Complete PVI will be achieved when all PV potentials within each antrum recorded by the high-density mapping catheter are abolished. The endpoint of the circumferential PVA ablation procedure is to achieve electrical bilateral PV isolation, that is, the PV potentials associated with atrial electrical activity cannot be recorded during sinus rhythm or CS pacing (entrance block). A waiting period of at least 20 min (after the last PV is isolated) will be used during which spontaneous PV reconnection will be related. , and tDemonstration of exit block (he by pacing in the PV cannot be and proving the absence of transmitted conduction to capture the atrium) may be performed but is not mandatory. Any organized AT observed during the procedure will be targeted as well.

Locations

Country	Name	City	State
China	Beijing Anzhen Hospital	Beijing	Beijing
China	Shengli Oilfield Central Hospital	Dongying	Shandong
China	Sun Yat-sen Memorial Hospital	Guangzhou	Guangdong
China	Sir Run Run Shaw Hospital	Hangzhou	Zhejiang
China	The First Affiliated Hospital of Harbin Medical University	Harbin	Heilongjiang
China	Shandong Provincial Hospital	Jinan	Shandong
China	The First Affiliated Hospital of Shandong First Medical University	Jinan	Shandong
China	Jiangsu Provincial Hospital	Nanjing	Jiangsu
China	Shanghai Renji Hospital	Shanghai	Shanghai
China	Taizhou Hospital of Zhejiang Province	Taizhou	Hangzhou
China	Wuhan Asia Heart Hospital	Wuhan	Hubei
China	Fuwai Central China Cardiovascular Hospital	Zhengzhou	Henan

Sponsors (5)

Lead Sponsor	Collaborator
Beijing Anzhen Hospital	Fukuoka University, Heart Health Research Centre, The George Institute for Global Health, Australia, The George Institute for Global Health, China

Country where clinical trial is conducted

China, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	The recurrence rate of atrial tachycardia arrhythmias	freedom from any documented atrial arrhythmia after a 3-months post-ablation blanking period, including AF, AT, and AFL, for more than 30 seconds in the absence of antiarrhythmic drug (AAD) therapy.	1 year
Secondary	Freedom from AF/AT with or without AADs	Time to the first occurrence of AF, AT in the presence of AAD therapy after one ablation procedure.	1 year
Secondary	Freedom from AF/AT off AADs	Recurrent AT/AFL over 30 seconds after a 3-month post-ablation blanking period in the absence of AAD	1 year
Secondary	Freedom from AF off AADs	Recurrent AF over 30 seconds after a 3-month post-ablation blanking period in the absence of AAD	1 year
Secondary	AF burden	AF burden (% time) on continuous monitoring during 12 months after the 3-months blanking period,	1 year
Secondary	Freedom from AF/AT after multiple procedures	freedom from any documented atrial arrhythmia (AF, AT, and AFL) of more than 30 seconds, after repeated ablation1 or 2 ablation procedures, including AF, AT, and AFL, for more than 30 seconds on/off AADs.	1 year
Secondary	Incidence of procedural complications	cardiac tamponade or perforation, phrenic nerve injury, acute coronary occlusion, leading to death, intervention required, or prolonged hospitalization, strokes /thromboembolism related to AF ablation, pulmonary vein stenosis, left atrial oesophageal fistula, and vascular complications requiring intervention (e.g., pseudoaneurysm, arteriovenous fistula).	Within 1 month after the procedure
Secondary	AFEQT score change between baseline and 12 month	Quality of life assessed by AF effect on quality-of-life (AFEQT) questionaire	1 year
Secondary	EQ5D score change between baseline and 12 month	Quality of life assessed by EuroQol 5-dimension (EQ5D) scale	1 year