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临床试验/NCT01477138
NCT01477138Unknown不适用

Comparison of Right Ventricular Septal Pacing to Minimized Right Ventricular Septal Stimulation in Patients With Sick Sinus Syndrome

Klinikum Nürnberg1 个研究点 分布在 1 个国家目标入组 126 人开始时间: 2011年7月最近更新:
适应症

试验速览

阶段
不适用
入组人数
126
试验地点
1
主要终点
end-systolic LV volume

研究概览

简要总结

Background:

  • Potential negative effects of pacing in the RV-apex are well documented
  • However, study results comparing septal / RVOT-pacing versus RV-apical pacing controversial.
  • The optimal pacing mode in SSS (DDDR versus AAIR) is unclear, as the DDD (R) mode with an AV delay ≤ 220 ms should be the preferred pacing mode, according to the DANPACE trial [DANPACE, ESC 2010, Stockholm].

Aim:

  • to evaluate chronic effects of proven right ventricular septal compared to minimized right ventricular septal pacing in patients with SSS

Inclusion criterion:

-Pacemaker indication according to current guidelines: sick sinus syndrome (SSS)

Exclusion criteria:

  • Life expectancy < 2 years
  • Age <18 years
  • Noncompliance with regard to participation in the study
  • Pregnancy
  • AV block ° 2 and higher
  • Permanent atrial fibrillation
  • Heart failure NYHA III and IV, reduced LV-EF <40%
  • ICD indication
  • Acute coronary syndrome. PCI or CABG <3 months
  • Heart transplant
  • Placement of septal RV electrode is not possible

Study design:

  • Prospective, monocentric, randomized, double-blinded
  • Run-in phase: for weeks AAI [R]-DDD [R]
  • Randomization: two groups A) septal right ventricular chamber pacing: mode DDD [R] versus B) Reduction of unnecessary ventricular pacing: AAI [R]-DDD [R].
  • FU: 6 and 12-months

Primary endpoints:

-LV ejection fraction and end-systolic LV volume after 12 months.

Secondary endpoints:

-LV end-diastolic volume, TAPSE, parameters of dyssynchrony (SPWMD, LV-PEP, IVMD), AF-burden, % ventricular pacing, CPX: peak oxygen consumption (peak VO2), VO2 AT, VO2/HR, VE/VCO2 slope; QoL scores (SF-36) after 12 months.

Statistics/sample size estimation:

In order to detect a difference in LVEF of 5% and for LV-ESV of 5 mL between the 2 groups after 12 months:

  • 90% power/alpha 5%: 84 patients per group

  • 80% power/alpha 5%: 63 patients per group

  • 10% for compensation of drop-outs / patients lost of follow-up. Two-sided 5% type 1 error Analysis intention-to-treat and based on the finally programmed pacing mode.

Material

  • PG: market released dual chamber pacemakers with the ability to pace AAI(R) -DDD(R)
  • pacing leads: market-released standard active electrodes
  • RV electrode: septal verified under multi-level screening (RAO/LAO) and ECG (LBBB narrow <150 ms / inferior axis)

详细描述

Background:

  • Potential negative effects of pacing in the RV-apex are well documented
  • Asynchronous ventricular activation
  • reduction of systolic and diastolic LV function
  • Experimental data: histological changes
  • Asymmetric LV hypertrophy and thinning
  • However, study results comparing septal / RVOT-pacing versus RV-apical pacing controversial:
  • Acute versus chronic
  • Small number of cases, uncontrolled, unblinded,
  • Brief periods of observation in the cross-over design (3 months)
  • "RVOT" often summarizes different stimulation sites: high RVOT, lateral, septal. Actually only limited data with proven septal stimulation
  • No objective performance assessment (CPX)
  • Assessment of alternative stimulation site previously RVOT versus RV-apex,
  • ventricular pacing compared to ventricular pacing, then tested a potential harm to another
  • The question of the optimal pacing mode of patients with SSS (DDDR versus AAIR) appears to be open again. While in Germany, two-chamber systems with AAI [R] mode with ventricular back-up are used, should the DDD (R) mode with an AV delay ≤ 220 ms be the preferred pacing mode, according to the results of the DANPACE trial for patients with SSS [DANPACE, ESC 2010, Stockholm].

Aim:

  • to evaluate chronic effects of proven right ventricular septal compared to minimized right ventricular septal pacing in patients with SSS

Inclusion criterion:

研究设计

研究类型
Observational
观察模型
Case Control
时间视角
Prospective

入排标准

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

入选标准

  • Pacemaker indication according to current guidelines: sick sinus syndrome (SSS)

排除标准

  • Life expectancy <2 years
  • Age < 18 years
  • Noncompliance with regard to participation in the study
  • Pregnancy
  • AV block ° 2 and higher
  • Permanent atrial fibrillation
  • Heart failure NYHA III and IV, reduced LV-EF < 40%
  • ICD indication
  • Acute coronary syndrome. PCI or CABG < 3 months
  • Heart transplant
  • Placement of septal RV electrode is not possible

结局指标

主要结局

end-systolic LV volume

时间窗: at randomisation and after 12 months

left ventricular ejection fraction (LV-EF)

时间窗: at randomisation and after 12 months

TTE, Simpson, biplane

次要结局

  • TAPSE(at randomisation and after 12 months)
  • echocardiographic parameter of dyssynchrony(at randomisation and after 12 months)
  • peak VO2, VO2 AT, VO2/HR, VE/VCO2 slope(at randomisation and after 12 months)
  • quality of life-scores(at randomisation and after 12 months)
  • AF burden(at randomisation and after 12 months)
  • % ventricular pacing(at randomisation and after 12 months)
  • LV end diastolic volume(at randomisation and after 12 months)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Natalia Rohr

Natalia Rohr

Klinikum Nürnberg

研究点 (1)

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