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Non-sedation Versus Sedation With a Daily Wake-up Trial in Critically Ill Patients Receiving Me-chanical Ventilation - Effects on Cognitive Function

Primary Purpose

Delirium, Cognition Disorders

Status
Completed
Phase
Not Applicable
Locations
Denmark
Study Type
Interventional
Intervention
Non-sedation
Control: Sedation
Sponsored by
Palle Toft
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional other trial for Delirium focused on measuring Respiration, artificial, Critcal care

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Endotracheally intubated
  • Expected time on ventilator > 24 hours
  • Age ≥ 18 years
  • Informed consent

Exclusion Criteria:

  • Severe head trauma where therapeutic coma is indicated
  • Therapeutic hypothermia where therapeutic coma is indicated
  • Status epilepticus where therapeutic coma is indicated
  • Patient has participated in the study before
  • Patient is transferred from another ICU with length of stay > 48 hours
  • Patient is comatose at admission
  • PaO2/FiO2 ≤ 9, if sedation is necessary for oxygenation
  • Patient does not speak Danish, swedish or norwegian at a reasonable level

Sites / Locations

  • Lillebaelt Hospital, Kolding, Intensive Care Unit

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Non-sedation

Sedation

Arm Description

Non-sedation supplemented with pain management during mechanical ventilation.

Current gold standard: Sedation with a daily wake-up trial.

Outcomes

Primary Outcome Measures

Cognitive function
Cognitive t-score, in percentage, difference between the two groups. The t-score for each patient will be diagnosed by the neuropsycologist at a personal interview and use of following tests: Span of numbers Coding test Trailmaking A+B Rey auditory verbal learning test (immediate, recall) Rey-Ostherrieth complex figure test (immediate, recall, recognition) Word finding test (S-word, animals) Stroop test (congruent+incongruent)

Secondary Outcome Measures

Attention/concentration
T-score in the two groups for the cognitive domaine attention/concentration
Learning/memory
t-score in the two groups for the cognitive domaine: learning/memory
Executive dysfunction
t-score in the two groups for the cognitive domaine: executive dysfunction
Mental pace
t-score in the two groups for the cognitive domaine: mental pace
Hypoactive delirium
Occurrence of hypoactive delirium (RASS ≤ 0, CAM-ICU positive) in each group related to cognitive function at follow up
Agitated delirium
Occurrence of agitated delirium (RASS ≥ +2, CAM-ICU positive) in each group related to cognitive function at follow up

Full Information

First Posted
January 10, 2014
Last Updated
March 14, 2019
Sponsor
Palle Toft
Collaborators
Kolding Sygehus, University of Southern Denmark, The Danish Council for Strategic Research
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1. Study Identification

Unique Protocol Identification Number
NCT02035436
Brief Title
Non-sedation Versus Sedation With a Daily Wake-up Trial in Critically Ill Patients Receiving Me-chanical Ventilation - Effects on Cognitive Function
Official Title
Substudy of the NONSEDA Trial (NCT01967680): Non-sedation Versus Sedation With a Daily Wake-up Trial in Critically Ill Patients Receiving Me-chanical Ventilation - Effects on Cognitive Function
Study Type
Interventional

2. Study Status

Record Verification Date
March 2019
Overall Recruitment Status
Completed
Study Start Date
January 2014 (Actual)
Primary Completion Date
June 2017 (Actual)
Study Completion Date
March 2019 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Palle Toft
Collaborators
Kolding Sygehus, University of Southern Denmark, The Danish Council for Strategic Research

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Through many years, the standard care has been to use continuous sedation of critically ill patients during mechanical ventilation. However, preliminary randomised clinical trials indicate that it is beneficial to reduce the sedation level in these patients. The NONSEDA trial is an investigator-initiated, randomised, clinical, parallel-group, multinational, superiority trial designed to include 700 patients from at least six ICUs in Denmark, Norway and Sweden, comparing no sedation with sedation and a daily wake-up trial during mechanical ventilation. This is a substudy of the NONSEDA trial, concerning 250 patients included at trialsite Kolding, Denmark. The aim of the substudy is to assess the effects of no sedation on delirium during admission and cognitive function after discharge from ICU. Our hypothesis is that critically ill patients who are not sedated during mechanical ventilation will have better cognitive function after discharge.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Delirium, Cognition Disorders
Keywords
Respiration, artificial, Critcal care

7. Study Design

Primary Purpose
Other
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Investigator
Allocation
Randomized
Enrollment
205 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Non-sedation
Arm Type
Experimental
Arm Description
Non-sedation supplemented with pain management during mechanical ventilation.
Arm Title
Sedation
Arm Type
Active Comparator
Arm Description
Current gold standard: Sedation with a daily wake-up trial.
Intervention Type
Other
Intervention Name(s)
Non-sedation
Intervention Description
Patients are awake or have natural sleep during mechanical ventilation. Pain is treated with morphine iv.
Intervention Type
Other
Intervention Name(s)
Control: Sedation
Intervention Description
Continuous iv-sedation (propofol first 48 hours, from then midazolam) to Ramsey 3-4 with a daily wake up attempt, where sedation is stopped until patient is awake.
Primary Outcome Measure Information:
Title
Cognitive function
Description
Cognitive t-score, in percentage, difference between the two groups. The t-score for each patient will be diagnosed by the neuropsycologist at a personal interview and use of following tests: Span of numbers Coding test Trailmaking A+B Rey auditory verbal learning test (immediate, recall) Rey-Ostherrieth complex figure test (immediate, recall, recognition) Word finding test (S-word, animals) Stroop test (congruent+incongruent)
Time Frame
3 months after discharge from ICU
Secondary Outcome Measure Information:
Title
Attention/concentration
Description
T-score in the two groups for the cognitive domaine attention/concentration
Time Frame
3 months after discharge from ICU
Title
Learning/memory
Description
t-score in the two groups for the cognitive domaine: learning/memory
Time Frame
3 months after discharge from ICU
Title
Executive dysfunction
Description
t-score in the two groups for the cognitive domaine: executive dysfunction
Time Frame
3 months after discharge from ICU
Title
Mental pace
Description
t-score in the two groups for the cognitive domaine: mental pace
Time Frame
3 months after discharge from ICU
Title
Hypoactive delirium
Description
Occurrence of hypoactive delirium (RASS ≤ 0, CAM-ICU positive) in each group related to cognitive function at follow up
Time Frame
3 months after discharge from ICU
Title
Agitated delirium
Description
Occurrence of agitated delirium (RASS ≥ +2, CAM-ICU positive) in each group related to cognitive function at follow up
Time Frame
3 months after discharge from ICU

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Endotracheally intubated Expected time on ventilator > 24 hours Age ≥ 18 years Informed consent Exclusion Criteria: Severe head trauma where therapeutic coma is indicated Therapeutic hypothermia where therapeutic coma is indicated Status epilepticus where therapeutic coma is indicated Patient has participated in the study before Patient is transferred from another ICU with length of stay > 48 hours Patient is comatose at admission PaO2/FiO2 ≤ 9, if sedation is necessary for oxygenation Patient does not speak Danish, swedish or norwegian at a reasonable level
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Helene Joergensen, MD
Organizational Affiliation
Lillebaelt Hospital, Kolding
Official's Role
Principal Investigator
Facility Information:
Facility Name
Lillebaelt Hospital, Kolding, Intensive Care Unit
City
Kolding
ZIP/Postal Code
6000
Country
Denmark

12. IPD Sharing Statement

Citations:
PubMed Identifier
27250658
Citation
Nedergaard HK, Jensen HI, Stylsvig M, Lauridsen JT, Toft P. Non-sedation versus sedation with a daily wake-up trial in critically ill patients recieving mechanical ventilation - effects on long-term cognitive function: Study protocol for a randomized controlled trial, a substudy of the NONSEDA trial. Trials. 2016 Jun 1;17(1):269. doi: 10.1186/s13063-016-1390-5.
Results Reference
derived

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Non-sedation Versus Sedation With a Daily Wake-up Trial in Critically Ill Patients Receiving Me-chanical Ventilation - Effects on Cognitive Function

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