跳至主要内容
临床试验/NCT01628172
NCT01628172已完成不适用

Renal Sympathetic Denervation for the Management of Chronic Hypertension

Vivek Reddy4 个研究点 分布在 1 个国家目标入组 96 人开始时间: 2011年1月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
96
试验地点
4
主要终点
Change in 24-hour ambulatory BP

研究概览

简要总结

Despite the development of numerous drug therapies designed to treat hypertension, it remains a considerable and poorly managed health, social and economic burden. For various reasons, including the significant health care costs of treatment, there are estimates that up to 65% of hypertensive patients have untreated and/or uncontrolled blood pressure (BP).

Aside from its impact on renal function, chronic hypertension significantly increases the risk for stroke, coronary artery disease, heart failure, and vascular disease. It is believed to be involved in the progression of cardiac arrhythmias. This link between hypertension and cardiovascular health has been well described; as has their combined effect on the aging and obesity-battling Western world.

The recently published results of the Symplicity HTN-2 trial (Renal sympathetic denervation in patients with treatment resistant hypertension) establishing the therapeutic benefit of catheter-based renal sympathetic denervation for hypertension, have enormous potential for the management of a large and challenging patient population. The proposed, multicenter trial will attempt to confirm and expand on this promising data by conducting a double-blinded, placebo-controlled trial.

Patients may qualify to participate in this research study if their doctor has determined that they have drug-resistant, chronic hypertension.

Overall participation in this research study should be about 13 months which includes about 1 month to start the study procedure and 12 months of follow-up after the study procedure.

详细描述

Patients who qualify for the study and provide consent will undergo a renal angiogram in order to assess suitability for catheter-based renal sympathetic denervation. A renal angiogram is an x-ray study of the blood vessels in the kidney to evaluate for blockage, and abnormalities that could be affecting the blood supply to the kidney. It is performed by injecting contrast dye through a catheter (a tiny tube) into the blood vessels of the kidney. The study doctor will assess whether the renal arteries are suitable to receive catheter-based renal denervation.

Both groups will receive sedation or anesthesia prior to the beginning of the procedure.

The first group will undergo catheter-based sympathetic renal denervation. Renal Sympathetic Denervation is a procedure that uses a catheter probe inserted into the renal (kidney) artery that deactivates the nerves that are linked to high blood pressure.

The second group will only receive renal angiography without the delivery of ablative energy.

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
Single (Participant)

入排标准

年龄范围
18 Years 至 85 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • ≥ 18 and ≤ 85 years of age
  • Uncontrolled hypertension (defined as SBP ≥ 140 mmHg during 24Hr Ambulatory BP monitoring)
  • Current treatment with ≥ 3 anti-hypertensive drugs (including at least one diuretic)
  • Accessibility of renal vasculature
  • Ability to understand the requirements of the study
  • Willingness to adhere to study restrictions and comply with all post-procedural follow-up requirements

排除标准

  • Secondary cause of hypertension
  • White coat hypertension
  • Estimated GFR < 45
  • Type 1 Diabetes
  • Known renovascular abnormalities (eg, renal artery stenosis, previous renal artery stenting or angioplasty)
  • Life expectancy <1 year for any medical condition

结局指标

主要结局

Change in 24-hour ambulatory BP

时间窗: baseline and at 6 months

Differences in 24-hour ambulatory blood pressure measurements recorded at baseline and at 6 months for each patient.

次要结局

  • change in office BP(baseline, 6 months, and 12 months)
  • change in ambulatory BP(baseline and at 12 months)
  • Renal artery dimensions(baseline and at 6 months)
  • Creatinine(baseline and at 6 months)

研究者

发起方
Vivek Reddy
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Vivek Reddy

Director Cardiac Arrhythmia Service, Professor of Medicine

Icahn School of Medicine at Mount Sinai

研究点 (4)

Loading locations...

相似试验