Trial Review

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Trial details imported from ClinicalTrials.gov

For full trial details, please see the original record at https://clinicaltrials.gov/ct2/show/NCT00202319




Registration number
NCT00202319
Ethics application status
Date submitted
14/09/2005
Date registered
20/09/2005
Date last updated
20/09/2005

Titles & IDs
Public title
Effectiveness of Sedation Management in an Australian Intensive Care Unit
Scientific title
Evaluating the Effectiveness of Protocol Directed Sedation Management With Non-Protocol Directed Sedation Management on Mechanically Ventilated Patients in an Australian Intensive Care Unit.
Secondary ID [1] 0 0
2001.102
Universal Trial Number (UTN)
Trial acronym
Linked study record

Health condition
Health condition(s) or problem(s) studied:
Respiration Disorders 0 0
Condition category
Condition code

Intervention/exposure
Study type
Interventional
Description of intervention(s) / exposure
Treatment: Surgery - Sedation management protocol

Treatment: Surgery: Sedation management protocol
Intervention code [1] 0 0
Treatment: Surgery
Comparator / control treatment
Control group

Outcomes
Primary outcome [1] 0 0
Duration of Ventilation
Timepoint [1] 0 0
Secondary outcome [1] 0 0
Length of stay
Timepoint [1] 0 0
Secondary outcome [2] 0 0
Tracheostomy insertion rate
Timepoint [2] 0 0
Secondary outcome [3] 0 0
Self extubation rate
Timepoint [3] 0 0

Eligibility
Key inclusion criteria
- mechanically ventilated
Minimum age
17 Years
Maximum age
No limit
Sex
Both males and females
Can healthy volunteers participate?
No
Key exclusion criteria
- cardiac surgery patients

- those patients readmitted to the ICU who had been on the study during a previous
admission were excluded for any subsequent admissions.

Study design
Purpose of the study
Treatment
Allocation to intervention
Randomised controlled trial
Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
Methods used to generate the sequence in which subjects will be randomised (sequence generation)
Masking / blinding
Open (masking not used)
Who is / are masked / blinded?



Intervention assignment
Parallel
Other design features
Phase
Not Applicable
Type of endpoint/s
Statistical methods / analysis

Recruitment
Recruitment status
Completed
Data analysis
Reason for early stopping/withdrawal
Other reasons
Date of first participant enrolment
Anticipated
Actual
1/11/2001
Date of last participant enrolment
Anticipated
Actual
Date of last data collection
Anticipated
Actual
Sample size
Target
Accrual to date
Final
Recruitment in Australia
Recruitment state(s)
VIC
Recruitment hospital [1] 0 0
Royal Melbourne Hospital - Melbourne
Recruitment postcode(s) [1] 0 0
3050 - Melbourne

Funding & Sponsors
Primary sponsor type
Other
Name
Melbourne Health
Address
Country
Other collaborator category [1] 0 0
Other
Name [1] 0 0
University of Melbourne
Address [1] 0 0
Country [1] 0 0
Other collaborator category [2] 0 0
Other
Name [2] 0 0
Australian College of Critical Care Nurses
Address [2] 0 0
Country [2] 0 0
Other collaborator category [3] 0 0
Commercial sector/Industry
Name [3] 0 0
Abbott
Address [3] 0 0
Country [3] 0 0

Ethics approval
Ethics application status

Summary
Brief summary
Sedation is an important treatment when caring for the critically ill patient on a
respirator. Adequate sedation has been found to reduce stress, promote relaxation, induce
amnesia, improve the tolerance of the respirator, and generally assist nursing care. However
all sedation produces side effects for the patients. The aim of this study is to measure the
effectiveness of two approaches to sedation management in an Australian Intensive Care unit.
Trial website
https://clinicaltrials.gov/ct2/show/NCT00202319
Trial related presentations / publications
Public notes

Contacts
Principal investigator
Name 0 0
Tracey K Bucknall, RN PhD
Address 0 0
University of Melbourne
Country 0 0
Phone 0 0
Fax 0 0
Email 0 0
Contact person for public queries
Name 0 0
Address 0 0
Country 0 0
Phone 0 0
Fax 0 0
Email 0 0
Contact person for scientific queries



Summary Results

For IPD and results data, please see https://clinicaltrials.gov/ct2/show/NCT00202319