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临床试验/NCT00182416
NCT00182416已完成3 期

Second Canadian Trial of Physiologic Pacing (CTOPP II): Pilot Trial

Hamilton Health Sciences Corporation9 个研究点 分布在 1 个国家目标入组 300 人开始时间: 2004年5月最近更新:
适应症

试验速览

阶段
3 期
状态
已完成
入组人数
300
试验地点
9
主要终点
Feasibility of the trial

研究概览

简要总结

Pacemaker therapy has been recognized as effective for the control of sinus and atrio-ventricular (AV) node dysfunction. Single chamber pacing when compared with dual chamber pacing, has numerous advantages of low complication rates, lower cost, better longevity, with non-inferiority in the quality of life and hard outcomes proven in direct randomized comparisons. However, comparison between single and dual chamber pacers was never adequate, since not more then half of the patients in the trials were actually using pacemakers for the majority of the time. Routine dual chamber pacing using a right ventricle apical lead is also associated with significant increase in peri-operative and remote complications. Some of these complications may be related to ventricular desynchronization secondary to the pacing location, which is potentially avoidable by using biventricular pacing. A randomized trial which will compare single chamber rate responsive pacing to the best available modification of dual chamber pacing (biventricular pacing) in suitable patients is therefore warranted.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Double

入排标准

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

入选标准

  • Patient has symptomatic bradycardia and is a candidate for first pacemaker implantation
  • Patient has high risk of being pacemaker dependent by (at least one of the following):
  • Average heart rate of 60 or less on pre-implant Holter
  • Maximal heart rate of 60 in patient on telemetry monitoring 12 hrs preoperatively, when not under medications decreasing heart rate, or under chronic medical treatment inducing bradycardia, which is unlikely to be changed
  • First degree AV block with PR intervals > 300 ms, or second degree AV block at heart rates <= 80 bpm.
  • Dependence for 12 hrs when on temporary pacemaker set at 50 bpm if bradycardia is not secondary to medication, or under chronic medical treatment inducing bradycardia, which is unlikely to be changed.

排除标准

  • Age <= 65 years
  • Chronic Atrial Fibrillation
  • Indication for ICD
  • Non-cardiovascular death is likely to occur within 3 years
  • Geographical, social, or psychiatric reasons making follow-up problematic

结局指标

主要结局

Feasibility of the trial

Predictors of future pacemaker dependence

次要结局

未报告次要终点

研究者

申办方类型
Other

研究点 (9)

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