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临床试验/NCT01802255
NCT01802255撤回3 期

Study of the Safety of Administration of Sevoflurane for Long-term Critically Ill Patients Sedation Undergoing Mechanical Ventilation. Prospective, Controlled, Randomized, Multicenter, Clinical Trial.

F Javier Belda1 个研究点 分布在 1 个国家开始时间: 2013年3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
撤回
发起方
试验地点
1
主要终点
Maintenance of renal function.

研究概览

简要总结

Patients needing intensive care often require sedative drugs to reduce anxiety and agitation during ventilator care and invasive therapeutic and diagnostic procedures. At present there is no optimal sedative agent for these patients. The most commonly used sedative agents in intensive care units are midazolam and propofol. Both drugs have side effects of clinical importance.

At present, a viable alternative to intravenous sedation is inhalatory sedation. Sevoflurane, as other inhaled anesthetic agents, is sedative in low doses. A new simplified method of administration of isoflurane or sevoflurane has been developed. The Anesthetic Conserving Device is a modified heat-moisture exchanger (HME) that permits direct infusion of sevoflurane to the airway, where it is vaporized in an evaporator rod in the device.

However, the use of sevoflurane is limited to anesthesia and sedation lasting no more than 12 hours, since the possible renal problems posed by inorganic fluoride in prolonged operations remain the subject of controversy.

The primary aim (and primary hypothesis) of the current trial is to determine whether sevoflurane can be administered as a sedative drug for more than 48 hours without clinically relevant physiopathological effects on kidney and liver function.

Other end-points of the trial are to evaluate the quality of sedation of sevoflurane, in terms of sedation control, the rapidity and predictability of awakening, and the incidence of delirium in critical care patients.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Supportive Care
盲法
Double (Participant, 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

  • Signing of the informed consent document (patient or relatives).
  • Patient age 18 years or older.
  • Expected minimum duration of sedation: 48 hours.

排除标准

  • Chronic renal failure treated with replacement therapy (hemodialysis or peritoneal dialysis).
  • Acute kidney injury in Stage 3 of AKIN classification
  • Grade C hepatic Child-Pugh classification
  • Established Acute Respiratory Distress Syndrome (ARDS).
  • Central nervous system pathology with cognitive disorders that not allow performing the test of the study: severe dementia, Alzheimer's disease, depression, schizophrenia, acute stroke.
  • Head trauma with Glasgow <
  • Patient treated with antiepileptic drugs that must be maintained during the study period
  • Patients requiring the use of neuromuscular blocking agents during the infusion of study drug, except for the insertion of the endotracheal tube.
  • Epidural or spinal analgesia
  • Allergy or known hypersensitivity to any of the study drugs
  • Patients with known or suspected genetic susceptibility to malignant hyperthermia
  • Previous participation in this trial
  • Participation in another clinical trial within 4 weeks prior to selection.
  • Pregnant women

研究组 & 干预措施

Inhalatory sedation

Experimental

Sevoflurane given via AnaConDa for sedation minimum 48 hours

干预措施: Sevoflurane (Drug)

Intravenous sedation

Active Comparator

Midazolam given intravenously for sedation minimum 48 hours

干预措施: Midazolam (Drug)

结局指标

主要结局

Maintenance of renal function.

时间窗: Baseline. Posteriorly, every 12 hours for the full length of sedation. After sedation, every 24 hours up to one week

Measurements in plasma: creatinine and cystatin levels.

次要结局

  • Plasma pharmacokinetics of fluoride(Baseline. Posteriorly, every 12 hours for the full length of sedation. After sedation, every 24 hours up to one week)
  • Incidence of delirium(Baseline. Posteriorly, every 12 hours for the full length of sedation. After sedation, every 24 hours up to one week)
  • Assessment of liver function(Baseline. Posteriorly, every 12 hours for the full length of sedation. After sedation, every 24 hours up to one week)

研究者

发起方
F Javier Belda
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

F Javier Belda

Prof. Dr. F Javier Belda

Fundación para la Investigación del Hospital Clínico de Valencia

研究点 (1)

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