Perioperative Cognitive Function - Dexmedetomidine and Cognitive Reserve
Primary Purpose
Postoperative Delirium, PD, Postoperative Cognitive Dysfunction
Status
Completed
Phase
Phase 4
Locations
United States
Study Type
Interventional
Intervention
Precedex (Dexmedetomidine)
Placebo
Sponsored by
About this trial
This is an interventional treatment trial for Postoperative Delirium focused on measuring Postoperative Confusion, Postoperative Delirium, PD, Postoperative Cognitive Dysfunction, POCD
Eligibility Criteria
Inclusion Criteria:
- 68 and older
- elective major surgery under general anesthesia(major surgery is defined by a planned 2 day hospitalization)
- ASA physical status I-III
- capable and willing to consent
- MMSE > 20 (to exclude dementia)
Exclusion Criteria:
- Cardiac surgery
- Intracranial Surgery
- Emergency Surgery
- Patients with severe visual or auditory disorder/handicaps
- Illiteracy
- Patients with clinically significant Parkinson's Disease
- Patients not expected to be able to complete the 3 and 6 month postoperative tests
- Sick sinus syndrome without pacemaker
- Hypersensitivity to drug or class
- Current 2nd or 3rd degree AV block
- History of clinically significant bradycardia
- Contraindication to the use of an 2A-agonist
- Presence of a major psychiatric condition such as bipolar disorder, major depression, schizophrenia, or dementia
- ASA physical status IV or V
Sites / Locations
- University of Miami Medical Center
- Johns Hopkins Bayview Medical Center
- University of Maryland
- The Mayo Clinic
- St. Louis University
- Englewood Hospital & Medical Center
- Icahn School of Medicine at Mount Sinai
- University of North Carolina at Chapel Hill
- Cleveland Clinic
- Ohio State University
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Placebo Comparator
Arm Label
Precedex
Placebo
Arm Description
Precedex (Dexmedetomidine)
Placebo - normal saline
Outcomes
Primary Outcome Measures
Delirium Battery
Number of Participants with occurrence of Post-Operative Delirium in Post-Anesthesia Care Unit (PACU)
Secondary Outcome Measures
Neuropsychological Testing
Rate of change of cognitive function - data not collected because secondary analysis which was not performed
Intraoperative Bradycardia
Number of participants with intraoperative bradycardia
Intraoperative Hypotension
Number of participants with intraoperative hypotension
Intraoperative Hypertension
Number of participants with intraoperative hypertension
Length of Stay
Length of Stay (LOS) in the hospital
Full Information
NCT ID
NCT00561678
First Posted
November 19, 2007
Last Updated
March 22, 2018
Sponsor
Icahn School of Medicine at Mount Sinai
Collaborators
National Institute on Aging (NIA)
1. Study Identification
Unique Protocol Identification Number
NCT00561678
Brief Title
Perioperative Cognitive Function - Dexmedetomidine and Cognitive Reserve
Official Title
Perioperative Cognitive Function - Dexmedetomidine and Cognitive Reserve
Study Type
Interventional
2. Study Status
Record Verification Date
March 2018
Overall Recruitment Status
Completed
Study Start Date
February 2008 (undefined)
Primary Completion Date
May 2014 (Actual)
Study Completion Date
May 2014 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Icahn School of Medicine at Mount Sinai
Collaborators
National Institute on Aging (NIA)
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
Elderly patients who undergo anesthesia and non-cardiac surgery are subject to deterioration of brain function including the development of postoperative delirium (PD) and postoperative cognitive dysfunction (POCD). These disorders cause disability, distress for both patients and their families, are associated with other medical complications and account for significant additional health care costs. We currently use relatively primitive approaches to preventing and treating PD and POCD.
Dexmedetomidine is a drug used for sedation in critically ill patients that provides some pain relief and controls the bodies response to stress. The sedation produced by dexmedetomidine appears more similar to natural sleep than any other drug used for anesthesia and postoperative sedation. Data suggesting that dexmedetomidine can prevent delirium following cardiac surgery and the developing understanding of the causes of PD and POCD suggest that dexmedetomidine will be particularly effective.
Detailed Description
Postoperative Delirium or PD and Postoperative Cognitive Dysfunction or POCD are syndromes of central nervous system dysfunction that significantly complicate the recovery of a proportion of elderly patients following surgery.
Delirium is typically a transient syndrome characterized by a de-novo appearance of several pathognomonic behaviors, including disorientation, decreased attention span, sensory misperceptions, a waxing-and-waning type of confusion, and disorganized thinking. PD typically occurs on postoperative days 1 to 3 and is associated with prolonged hospital stays, increased risks for morbidity and mortality and significant health care expenditures.
The neuroendocrine stress response to surgery, including the immediate postoperative period, remains an important potential etiologic factor. In particular, our data suggests that stress in the immediate postoperative period is poorly controlled by all anesthetic techniques and the normal diurnal variation in cortisol is suppressed in subjects who develop POCD.
Dexmedetomidine is a highly selective alpha 2A agonist currently approved for sedation in the ICU. Dexmedetomidine produces analgesia, sympatholysis, and a light sedation characterized by easy arousal. Its action converges on the endogenous substrates for natural sleep to produce their sedative action, an effect that could prove beneficial to elderly postoperative patients.
We hypothesize that treatment with dexmedetomidine will diminish both PD and POCD. The essential proposition is that modulation of perioperative stress can ameliorate perioperative delirium and cognitive dysfunction.
Based on both the concept of cognitive reserve as well as clinical experience, there is concern that patients with preoperative cognitive impairment are particularly vulnerable to POCD. In general, such patients have been excluded from previous studies. This study is unique in that we will assess all participants for mild cognitive impairment prior to surgery. Assessment of the impact of preexisting cognitive impairment is a secondary aim. A broad goal of this interdisciplinary project is to evaluate POCD, which is primarily an anesthesia concept, in the more general context of dementing illness as explored by geriatric psychiatry.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Postoperative Delirium, PD, Postoperative Cognitive Dysfunction, POCD
Keywords
Postoperative Confusion, Postoperative Delirium, PD, Postoperative Cognitive Dysfunction, POCD
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigator
Allocation
Randomized
Enrollment
404 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Precedex
Arm Type
Experimental
Arm Description
Precedex (Dexmedetomidine)
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
Placebo - normal saline
Intervention Type
Drug
Intervention Name(s)
Precedex (Dexmedetomidine)
Other Intervention Name(s)
Dexmedetomidine
Intervention Description
0.5/ug/kg/hr Dexmedetomidine infusions will begin prior to the surgery (no loading dose), and will be maintained at 0.5 mcg/kg/hour throughout surgery and titrated postoperatively for 2 hours postoperatively.
Intervention Type
Drug
Intervention Name(s)
Placebo
Other Intervention Name(s)
Normal Saline
Intervention Description
0.5/ug/kg/hr Placebo infusions will begin prior to the surgery (no loading dose), and will be maintained at 0.5 mcg/kg/hour throughout surgery and titrated postoperatively for 2 hours postoperatively.
Primary Outcome Measure Information:
Title
Delirium Battery
Description
Number of Participants with occurrence of Post-Operative Delirium in Post-Anesthesia Care Unit (PACU)
Time Frame
Day 1
Secondary Outcome Measure Information:
Title
Neuropsychological Testing
Description
Rate of change of cognitive function - data not collected because secondary analysis which was not performed
Time Frame
at 3 months postoperatively
Title
Intraoperative Bradycardia
Description
Number of participants with intraoperative bradycardia
Time Frame
day 1
Title
Intraoperative Hypotension
Description
Number of participants with intraoperative hypotension
Time Frame
day 1
Title
Intraoperative Hypertension
Description
Number of participants with intraoperative hypertension
Time Frame
day 1
Title
Length of Stay
Description
Length of Stay (LOS) in the hospital
Time Frame
average 4 days
10. Eligibility
Sex
All
Minimum Age & Unit of Time
68 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
68 and older
elective major surgery under general anesthesia(major surgery is defined by a planned 2 day hospitalization)
ASA physical status I-III
capable and willing to consent
MMSE > 20 (to exclude dementia)
Exclusion Criteria:
Cardiac surgery
Intracranial Surgery
Emergency Surgery
Patients with severe visual or auditory disorder/handicaps
Illiteracy
Patients with clinically significant Parkinson's Disease
Patients not expected to be able to complete the 3 and 6 month postoperative tests
Sick sinus syndrome without pacemaker
Hypersensitivity to drug or class
Current 2nd or 3rd degree AV block
History of clinically significant bradycardia
Contraindication to the use of an 2A-agonist
Presence of a major psychiatric condition such as bipolar disorder, major depression, schizophrenia, or dementia
ASA physical status IV or V
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jeff Silverstein, MD
Organizational Affiliation
Icahn School of Medicine at Mount Sinai
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Miami Medical Center
City
Miami
State/Province
Florida
ZIP/Postal Code
33136
Country
United States
Facility Name
Johns Hopkins Bayview Medical Center
City
Baltimore
State/Province
Maryland
ZIP/Postal Code
21224
Country
United States
Facility Name
University of Maryland
City
College Park
State/Province
Maryland
ZIP/Postal Code
20742
Country
United States
Facility Name
The Mayo Clinic
City
Rochester
State/Province
Minnesota
ZIP/Postal Code
55905
Country
United States
Facility Name
St. Louis University
City
Saint Louis
State/Province
Missouri
ZIP/Postal Code
63104
Country
United States
Facility Name
Englewood Hospital & Medical Center
City
Englewood
State/Province
New Jersey
ZIP/Postal Code
07631
Country
United States
Facility Name
Icahn School of Medicine at Mount Sinai
City
New York
State/Province
New York
ZIP/Postal Code
10029
Country
United States
Facility Name
University of North Carolina at Chapel Hill
City
Chapel Hill
State/Province
North Carolina
ZIP/Postal Code
27599
Country
United States
Facility Name
Cleveland Clinic
City
Cleveland
State/Province
Ohio
ZIP/Postal Code
44195
Country
United States
Facility Name
Ohio State University
City
Columbus
State/Province
Ohio
ZIP/Postal Code
43210
Country
United States
12. IPD Sharing Statement
Citations:
PubMed Identifier
28593326
Citation
Deiner S, Luo X, Lin HM, Sessler DI, Saager L, Sieber FE, Lee HB, Sano M; and the Dexlirium Writing Group; Jankowski C, Bergese SD, Candiotti K, Flaherty JH, Arora H, Shander A, Rock P. Intraoperative Infusion of Dexmedetomidine for Prevention of Postoperative Delirium and Cognitive Dysfunction in Elderly Patients Undergoing Major Elective Noncardiac Surgery: A Randomized Clinical Trial. JAMA Surg. 2017 Aug 16;152(8):e171505. doi: 10.1001/jamasurg.2017.1505. Epub 2017 Aug 16.
Results Reference
result
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Perioperative Cognitive Function - Dexmedetomidine and Cognitive Reserve
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