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Completed

NCT Number: NCT01561378

Cardiac Surgery Neuroprotection Study in Elders

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.

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Key information

Age range

65 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

Albert Einstein College of Medicine - Montefiore Medical Center

The Bronx, New York, 10467, United States

About this study

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).

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

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

Exclusion criteria

  • 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

Treatment and study plan

Aspart insulin

Drug

40 IU of aspart insulin (200 microliters per nostril) will be administered intranasally using an intranasal mucosal atomizer device within 2 hours prior to surgery, and then four times a day for 7 days or until hospital discharge (whichever occurs first)

Other names: NovoLog

normal saline

Drug

200 microliters of normal saline will be administered per nostril using an intranasal mucosal atomizer device within 2 hours prior to surgery, and then four times a day for 7 days or until hospital discharge (whichever occurs first)

Other names: 0.9% sodium chloride solution

Intranasal mucosal atomizer device

Device

Insulin and placebo will be drawn into identical syringes. Nurses will administer the insulin or placebo by connecting the mucosal atomizer device (MAD) to the syringe, placing the MAD tip in the nostril and compressing the syringe plunger to spray atomized solution into the nasal cavity.

Other names: mucosal atomizer device, MAD

Primary outcomes

  1. Change From Baseline Cognitive Function

    Time frame: 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.

Secondary outcomes

  1. Delirium and Coma Free Days

    Time frame: 7 days

    Assessed using the Richmond Agitation Sedation Scale (RASS) and Confusion Assessment Method-ICU (CAM-ICU)

  2. Association Between Post-operative Delirium and Post-operative Cognitive Decline

    Time frame: 7 days, 6 weeks

  3. Hypoglycemia

    Time frame: 14 days

  4. Nasal Irritation

    Time frame: 14 days

  5. Survival

    Time frame: 30-day, 90-day

  6. ICU Length of Stay

    Time frame: 1 to 90 days

  7. Hospital Length of Stay

    Time frame: 1 to 90 days

Sponsors and collaborators

Lead sponsor

Albert Einstein College of Medicine

Other

Collaborators

  • National Institute on Aging (NIA)

Registry information

Official study title

Intranasal Insulin for Neuroprotection in Elderly Cardiac Surgery Patients

Acronym: CNS-Elders

Important dates

Study start
2012
Primary completion
2014
Study completion
2014
First posted
Mar 23, 2012
Registry last updated
Nov 10, 2021

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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