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临床试验/NCT00562692
NCT00562692终止3 期

Role of Natriuretic Peptides in the Treatment of Acutely Decompensated Heart Failure Patient With Obstructive Airways Disease

The Alfred1 个研究点 分布在 1 个国家目标入组 6 人开始时间: 2007年9月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
3 期
状态
终止
发起方
入组人数
6
试验地点
1
主要终点
To compare the need for and the length of time patients require non invasive ventilation when treated with nesiritide vs placebo.

研究概览

简要总结

Brain natriuretic peptide (BNP) is a useful therapy when treating patients with heart failure. As many of these patients also have airways disease it is important to determine if BNP also has a positive effect on their respiratory condition. The role of BNP in airways disease has never been studied although there is evidence to suggest that it will have a positive effect.

The current study is therefore a proof on concept study which will demonstrate whether BNP (nesiritide) will improve both heart failure and airflow obstruction in patient who have both.

The investigators are looking to enroll 40 patients with heart failure and airways disease who present to hospital emergency departments. Patients who consent and meet the entry criteria will be randomised to receive either nesiritide or placebo in addition to standard therapy. They will receive a bolus of study medication followed by a 4 hour infusion. Before, at hourly intervals and immediately following the infusion the following data will be collected:

  • dyspnoea score
  • respiratory rate
  • FEV1 (if able to be performed)
  • peak respiratory flow rates (PEFR, if able to be performed)
  • requirement for concomitant bronchodilator therapy
  • urinary GMP At all times during the study period and at the conclusion of the study patients will be provided with the best available therapy for their condition at the physicians' discretion.

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

入选标准

  • Males and females
  • Over 18 years of age
  • Confirmed written informed consent.
  • Acute decompensated heart failure based on physicians assessment and requiring treatment as per standard emergency department protocols for this condition.
  • Requirement for intravenous therapy of HF, e.g. diuretic, vasodilator.
  • COAD based on physician's assessment and requiring treatment as per standard emergency department protocols for this condition. Must have at least 2 of the following criteria:
  • history of smoking > 20 pack years,
  • prior history of PFTs within last 1 year consistent with COAD,
  • history of chronic cough and sputum production,
  • progressive dyspnea, episodes of acute bronchitis over at least 2 yrs

排除标准

  • Women lactating, pregnant or of childbearing potential not using 2 reliable contraceptive methods.
  • Patients who had received an investigational new drug within the last 4 weeks.
  • Patients with a history of a psychological illness or condition such as to interfere with the patient's ability to understand the requirements of the study.
  • SBP <90mmHg
  • Creatinine >0.25mmol/L
  • Sp02 < 80% on supplemental oxygen or known cor pulmonale with TR

研究组 & 干预措施

A

Experimental

Nesiritide

干预措施: Nesiritide (Drug)

B

Placebo Comparator

Placebo

干预措施: Placebo (Drug)

结局指标

主要结局

To compare the need for and the length of time patients require non invasive ventilation when treated with nesiritide vs placebo.

时间窗: 24 hours

次要结局

  • dyspnoea score respiratory rate FEV1 PEFR requirement for concomitant bronchodilator therapy BNP(24 hours)

研究者

发起方
The Alfred
申办方类型
Other
责任方
Principal Investigator
主要研究者

Henry Krum

Head Clinical Pharmacology

The Alfred

研究点 (1)

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