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临床试验/NCT06733012
NCT06733012招募中不适用

Splanchnic Nerve Modulation In Heart Failure (Splanchnic X)

Duke University1 个研究点 分布在 1 个国家目标入组 54 人开始时间: 2025年4月5日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
招募中
发起方
入组人数
54
试验地点
1
主要终点
Number of participants with cardiovascular death

研究概览

简要总结

Heart failure (HF) affects more than 6 million adults in the U.S. alone, with increasing prevalence. Cardiovascular congestion with resultant limitation in physical activity is the hallmark of chronic and decompensated HF. The current HF physiologic model suggests that congestion is the result of volume retention and, therefore, therapies (such as diuretics) have generally been targeted at volume overload. Yet therapeutic approaches to reduce congestion have failed to show significant benefit on clinical outcomes, potentially due to an untargeted approach of decongestive therapies. The investigators' preliminary work suggested a complimentary contribution of volume redistribution to the mechanism of cardiac decompensation. The investigators identified the splanchnic nerves as a potential therapeutic target and showed that short-term interruption of the splanchnic nerve signaling could have favorable effects on cardiovascular hemodynamics and symptoms.

As part of the investigators' proposal, the investigators will test the safety and efficacy of prolonged splanchnic nerve block in a randomized, controlled, blinded study in patients with HF and reduced ejection fraction (HFrEF). The results will help test the hypothesis of volume redistribution as a driver of cardiovascular congestion and functional limitations and pave the way for splanchnic nerve blockade as a novel therapeutic approach to HF.

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
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

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

  • •Age > 18 years
  • •Established diagnosis of HFrEF with left ventricular ejection fraction <50%
  • •NYHA II-III symptoms
  • •Stable HF drug regimen for the preceding 1 month
  • •Wedge pressure >/=15 mmHg at rest or >/=20 mmHg with peak stress on the initial invasive exercise testing
  • •Glomerular filtration rate ≥ 15 mL/min per 1.73 m2
  • •Heart rate with activity such as the 6 min walk increases by at least 10 beats

排除标准

  • •Type I myocardial infarction within 3 months
  • •Infiltrative (i.e., amyloid) or hypertrophic cardiomyopathy
  • •Uncontrolled atrial (heart rate >100bpm) or ventricular arrhythmia
  • •Chronic oxygen use >2L
  • •Hypersensitivity to albumin and pregnancy
  • •History or scoliosis
  • •Orthostatic hypotension (including a drop of pulse pressure with standing of more than 10)

研究组 & 干预措施

Splanchnic nerve ablation

Experimental

Catheter based ablation on the right greater splanchnic nerve

干预措施: Splanchnic nerve block (Device)

Sham control

Sham Comparator

Sham-control procedure

干预措施: Sham-control procedure (Other)

结局指标

主要结局

Number of participants with cardiovascular death

时间窗: 1 month post intervention

Number of participants with stroke

时间窗: 1 month post intervention

Number of participants with acute myocardial infarction

时间窗: 1 month post intervention

Number of participants with major vascular complications resulting prolonged hospitalization or surgical intervention

时间窗: 1 month post intervention

Change in exercise pulmonary capillary wedge pressure (PCWP) post splanchnic nerve block (SNB)

时间窗: Baseline to 3 months post splanchnic nerve block (SNB)

Pulmonary capillary wedge pressure (PCWP) is measured by inserting a catheter with a balloon tip into a central vein and advancing it into a branch of the pulmonary artery. The catheter measures changing pressures in the pulmonary vessels. The upper limit of normal for PCWP is 12 mm Hg.

次要结局

  • Change in N terminal pro brain natriuretic protein (NT-proBNP) level(Baseline, 1, 3, 6, and 12 months)
  • Change in peak VO2 (oxygen uptake)(Baseline, 1, 3, 6, and 12 months)
  • Change in pulmonary arterial mean pressure(Baseline to 3 months)
  • Change in 6-minute walk test (6MWT)(Baseline, 1, 3, 6, and 12 months)
  • Change in echocardiographic parameters - ejection fraction (EF)(Baseline, 1, 3, and 6 months)
  • Change in echocardiographic parameters - right ventricular end diastolic diameter(Baseline, 1, 3, and 6 months)
  • Change in left ventricle to left atrial volume ratio (LVLAVR)(Baseline, 1, 3, and 6 months)
  • Change in diastolic function as measured with lateral wall e' and E/e'(Baseline, 1, 3, and 6 months)

研究者

发起方
Duke University
申办方类型
Other
责任方
Sponsor

研究点 (1)

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