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临床试验/NCT04180540
NCT04180540已完成不适用

A Randomized Comparison of Percutaneous Closure to Manual Compression for Hemostasis of Multiple Venous Access Sites Among Patients Undergoing Catheter Ablation for Atrial Fibrillation

Michael S. Lloyd2 个研究点 分布在 1 个国家目标入组 109 人开始时间: 2020年1月22日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
109
试验地点
2
主要终点
Time to Hemostasis

研究概览

简要总结

This a prospective randomized trial occurring in patients undergoing routine ablation for atrial fibrillation as standard of care. The purpose of this study is to determine if using a small internal suture (or "stitch") facilitates faster times to hemostasis (stopping bleeding) after removing intravenous sheaths (special IVs that are used for ablation procedures) after an atrial fibrillation ablation procedure. The device used to place the stitch is PerClose Proglide and is an already FDA-approved technology for closing these IV sites. The study will also determine if it is safe to get up and walk sooner than what is considered typical after closing these IV sites with the PerClose device. Participants will be randomized in a 1:1 ratio to either manual compression or use of the PerClose for hemostasis at the end of the ablation procedure. The length of follow-up will be up to 30 days at routine clinical follow-up after the procedure.

详细描述

Radiofrequency ablation and cryoablation for treatment of atrial fibrillation (AF) using percutaneous venous access at the groin is one of the most common procedures performed by cardiac electrophysiologists. However, compared to other catheter-based interventions, patients undergoing AF ablation pose a unique set of challenges. First, AF ablation requires multiple points of transfemoral venous access with large diameter sheaths, ranging in size from 8 French gauge (F) to 14F for cryoablation procedures. Second, operators are forced to balance the competing risk of thrombosis and bleeding in these patients. In order to minimize the risk of intraprocedural thrombosis, anticoagulation with heparin with a goal anticoagulation time (ACT) >300-350 seconds is necessary. However, operators typically require ACTs to normalize prior to removal of sheaths and manual compression, which significantly delays hemostasis and ambulation. While reversal agents are an option, there is currently clinical equipoise on their role and safety in this setting and they require additional time to exert their full effect. Lastly, patients require at least 1-2 months of therapeutic oral anticoagulation after the procedure to mitigate ongoing stroke risk. These factors culminate in longer times to hemostasis and ambulation and raise concerns for post-procedure access related complications for patients undergoing AF ablation. PerClose Proglide has recently gained FDA approval for closure of percutaneous venous access sites for catheter-based interventions and remains the only commercially available solution for access sites >14F inner diameter. Percutaneous closure of venotomy sites may facilitate rapid hemostasis without the need for reversal of anticoagulation, potentially attenuating bleeding risk. Additionally, typical bedrest times after percutaneous closure are based on data derived from arterial closure. Prior limited data, as well as frequent anecdotal reports, have suggested that earlier ambulation may be feasible. Because the venous circulation is a lower pressure system, it is possible that earlier than standard ambulation times after PerClose is both safe and feasible. However, a rigorous prospective investigation of the PerClose Proglide device in the context of AF ablation has not been performed.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Supportive Care
盲法
None

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •undergoing elective atrial fibrillation ablation at Emory University Hospital or Emory University Hospital Midtown

排除标准

  • •women who are pregnant (based on standard pre-procedure pregnancy test)
  • •patients who are not able to ambulate pre-procedure
  • •patients who are unable to provide informed consent

研究组 & 干预措施

Percutaneous Closure

Experimental

Participants randomized to undergo percutaneous closure with PerClose after radiofrequency ablation or cryoablation for treatment of atrial fibrillation.

干预措施: Percutaneous Closure (Device)

Manual Compression

Active Comparator

Participants randomized to undergo manual compression after radiofrequency ablation or cryoablation for treatment of atrial fibrillation.

干预措施: Manual Compression (Other)

结局指标

主要结局

Time to Hemostasis

时间窗: Day 1

Starting from sheath pull, time (in minutes) to hemostasis will be compared between study arms.

次要结局

  • Time to Ambulation(Day 1)
  • Procedure Length(Day 1)
  • Pain Medication Needs(Day 1)
  • Costs(Day 30)
  • Short-form Inguinal Pain Questionnaire Score(Day 30)
  • Patient Satisfaction(Day 1 and Day 30)
  • Number of Nursing Encounters(Day 1)
  • Number of Complications(Day 30)

研究者

发起方
Michael S. Lloyd
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Michael S. Lloyd

Associate Professor

Emory University

研究点 (2)

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