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临床试验/NCT01561378
NCT01561378已完成2 期

Intranasal Insulin for Neuroprotection in Elderly Cardiac Surgery Patients

Albert Einstein College of Medicine1 个研究点 分布在 1 个国家目标入组 22 人开始时间: 2012年8月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
2 期
状态
已完成
入组人数
22
试验地点
1
主要终点
Change From Baseline Cognitive Function

研究概览

简要总结

The goal of this study is to determine the potential ability of intranasal insulin to prevent post-operative cognitive decline and post-operative delirium in an elderly cardiac surgery population.

详细描述

Nearly half of all intensive care unit (ICU) admissions consist of adults > 65 years old, an age group that is at high risk for developing cognitive decline and delirium in the ICU. Over 50% and 70% of critically ill cardiac surgery patients develop post-operative delirium (POD) and post-operative cognitive decline (POCD), respectively. These two forms of acute cognitive dysfunction are associated with increased mortality and poor functional recovery. While distinct conditions, POD has been associated with the subsequent development of POCD, suggesting a mechanistic link.

No proven pharmacologic treatments targeting the prevention of both POD and POCD in elderly patients exist to date. Recent data suggest that insulin administered into the central nervous system via intranasal delivery improves cognitive function in elderly patients with Alzheimer's disease and mild cognitive impairment. However, its utility in preventing POD and POCD in elderly critically ill patients has not been investigated.

The hypothesis of this study is that intranasal insulin can prevent POD and POCD in elderly critically ill patients admitted to the intensive care unit after undergoing cardiac surgery. To test this hypothesis, this randomized, placebo-controlled, double-blinded Phase II study will enroll 60 patients >= 65 years old undergoing elective coronary artery bypass graft and/or valve surgery requiring cardiopulmonary bypass, and will treat them with either 40 IU of aspart insulin or placebo intranasally before surgery and then four times a day for 7 days or until hospital discharge (whichever occurs first).

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Prevention
盲法
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

入排标准

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

入选标准

  • elderly patients (>=65 years old)
  • undergoing elective coronary artery bypass graft and/or valve surgery requiring cardiopulmonary bypass
  • English or Spanish-speaking

排除标准

  • severe dementia, neurodegenerative, or psychiatric disease that prevents patient from living independently at baseline
  • emergent surgery
  • inability to perform cognitive testing (i.e. difficulty hearing or inability to speak)
  • contraindications to intranasal administration of medication

研究组 & 干预措施

Insulin

Experimental

Aspart Insulin 40 IU intranasal spray via intranasal mucosal atomizer device, four times a day for 7 days or until hospital discharge, whichever occurs first

干预措施: Aspart insulin (Drug)

Insulin

Experimental

Aspart Insulin 40 IU intranasal spray via intranasal mucosal atomizer device, four times a day for 7 days or until hospital discharge, whichever occurs first

干预措施: Intranasal mucosal atomizer device (Device)

Normal saline

Placebo Comparator

Normal saline (0.9% sodium chloride solution) intranasal spray via intranasal mucosal atomizer device, four times a day for 7 days or until hospital discharge, whichever occurs first

干预措施: Normal saline (Drug)

Normal saline

Placebo Comparator

Normal saline (0.9% sodium chloride solution) intranasal spray via intranasal mucosal atomizer device, four times a day for 7 days or until hospital discharge, whichever occurs first

干预措施: Intranasal mucosal atomizer device (Device)

结局指标

主要结局

Change From Baseline Cognitive Function

时间窗: 6-weeks

Assessed using a battery of cognitive tests which test the following four domains: 1) executive function, 2) verbal memory, 3) attention and concentration, 4) language. Cognitive testing will be performed at the following time points: baseline (1-2 weeks prior to surgery) and 6 weeks after discharge.

次要结局

  • Survival(30-day, 90-day)
  • Association Between Post-operative Delirium and Post-operative Cognitive Decline(7 days, 6 weeks)
  • Nasal Irritation(14 days)
  • ICU Length of Stay(1 to 90 days)
  • Delirium and Coma Free Days(7 days)
  • Hypoglycemia(14 days)
  • Hospital Length of Stay(1 to 90 days)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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