Trial Review

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Trial registered on ANZCTR


Registration number
ACTRN12620001208998
Ethics application status
Approved
Date submitted
5/10/2020
Date registered
13/11/2020
Date last updated
13/11/2020
Date data sharing statement initially provided
13/11/2020
Type of registration
Retrospectively registered

Titles & IDs
Public title
Measuring the impact of anaesthetic drug volume during surgery
Scientific title
MEasuring the impact of Anaesthetic drug volumeS on intra-operative flUid balance duRing prolonged abdominal surgEry (MEASURE)
Secondary ID [1] 302469 0
Nil known
Universal Trial Number (UTN)
U1111-1259-2094
Trial acronym
MEASURE
Linked study record

Health condition
Health condition(s) or problem(s) studied:
Pancreaticoduodenectomy 319300 0
Anaesthesia medications 319301 0
Condition category
Condition code
Anaesthesiology 317267 317267 0 0
Anaesthetics
Surgery 317268 317268 0 0
Other surgery
Cancer 317269 317269 0 0
Pancreatic
Oral and Gastrointestinal 317270 317270 0 0
Other diseases of the mouth, teeth, oesophagus, digestive system including liver and colon

Intervention/exposure
Study type
Observational
Patient registry
False
Target follow-up duration
Target follow-up type
Description of intervention(s) / exposure
There is no participant involvement. Only the de-identified hospital medical record of patients who have undergone pancreaticoduodenectomy (Whipple's operation) at the Austin Hospital from 1st Jan 2010 to 1st June 2020 will be reviewed.
Intervention code [1] 318761 0
Not applicable
Comparator / control treatment
No control group
Control group
Uncontrolled

Outcomes
Primary outcome [1] 325326 0
The primary outcome will be the volume (measured in milliliters) of intravenous anaesthesia medications and infusions administered intraoperatively in adult patients undergoing pancreaticoduodenectomy. This outcome will be obtained by extracting this data from the intraoperative anaesthesia medical record.
Timepoint [1] 325326 0
During the intraoperative period i.e. from anaesthesia induction to completion of surgery.
Secondary outcome [1] 387511 0
The secondary outcome will be the intraoperative fluid balance (measured in milliliters).

Intraoperative fluid balance will be calculated using the following formula: Fluid input (sum of all anaesthesia medications + crystalloids + colloids + blood or blood products) minus Fluid output (sum of all fluid loses i.e. urine output + blood loss + nasogastric loss). This outcome will be obtained by extracting this data from the intraoperative anaesthesia medical record.

Timepoint [1] 387511 0
During the intraoperative period i.e. form anaesthesia induction to completion of surgery.
Secondary outcome [2] 387512 0
To analyse the association of anaesthesia medications on the development of postoperative complications.

Complications will be assessed using the Clavien-Dindo system, a validated tool for grading complications. This outcome will be obtained by reviewing data-linkage to the Austin hospital's medical records.
Timepoint [2] 387512 0
From completion of surgery (last surgical stitch) to hospital discharge.
Secondary outcome [3] 387513 0
To analyse the association of anaesthesia medications and hospital length of stay.

This outcome will be obtained by reviewing data-linkage to the Austin hospital's medical records.
Timepoint [3] 387513 0
Hospital length of stay will be calculated in days from completion of surgery to discharge from hospital. This outcome will be obtained by reviewing data-linkage to the Austin hospital's medical records.

Eligibility
Key inclusion criteria
Adult patients who underwent a pancreaticoduodenectomy between 1st January 2010 to 1st June 2020 for any indication at the Austin Hospital will be eligible. Any indication for pancreaticoduodenectomy will be considered. Both emergent and elective procedures will also be considered.
Minimum age
18 Years
Maximum age
No limit
Sex
Both males and females
Can healthy volunteers participate?
No
Key exclusion criteria
We will exclude the following patients:
1. Distal pancreatectomy
2. Central pancreatectomy
3. Total pancreatectomy

Study design
Purpose
Natural history
Duration
Longitudinal
Selection
Defined population
Timing
Retrospective
Statistical methods / analysis
Collected data will be arranged using Microsoft Excel (Microsoft Office 365 version 2008, Microsoft corp., WA, USA).

Statistical analysis will be performed using R version 4.0.0 (R Development Core Team, Vienna, Austria, 2020).

Missing data analysis will be applied to detect a greater than 5% missing rate of all variables. For variables with a missing rate lower than 5%, cases will be analysed as planned. For variables with a missing rate of over 5%, the multiple imputation method will be applied.

Normality tests will then be performed for all continuous variables using Q-Q plot. If these tests are violated, non-parametric statistical methods or log-transformation will be applied.

Paired and unpaired t-test, Spearman’s correlation analysis, and receiver-operator characteristic curve (ROC) analysis will be used to investigate the primary and secondary outcomes. The R packages of “pROC” and “plotROC” will be used for ROC analysis.

Data will be presented as mean ± standard deviation (SD) or median (IQR)[Max:Min] for continuous variables and number (percentile) for categorical variables. Comparative results will be presented with a P-value and corresponding effect size. A two-tailed P value below 0.050 or a Bonferonni’s corrected value will be considered to be statistically significant.

Recruitment
Recruitment status
Completed
Date of first participant enrolment
Anticipated
Actual
28/10/2020
Date of last participant enrolment
Anticipated
Actual
9/11/2020
Date of last data collection
Anticipated
Actual
10/11/2020
Sample size
Target
150
Accrual to date
Final
150
Recruitment in Australia
Recruitment state(s)
VIC
Recruitment hospital [1] 17736 0
Austin Health - Austin Hospital - Heidelberg

Funding & Sponsors
Funding source category [1] 306894 0
Hospital
Name [1] 306894 0
Department of Anaesthesia, Austin Health
Country [1] 306894 0
Australia
Primary sponsor type
Hospital
Name
Department of Anaesthesia, Austin Health
Address
Department of Anaesthesia, Austin Health, 145 Studley Road, Heidelberg VIC, 3084
Country
Australia
Secondary sponsor category [1] 307451 0
None
Name [1] 307451 0
Address [1] 307451 0
Country [1] 307451 0

Ethics approval
Ethics application status
Approved
Ethics committee name [1] 307050 0
Austin Health Human Research Ethics Committee
Ethics committee address [1] 307050 0
Ethics committee country [1] 307050 0
Australia
Date submitted for ethics approval [1] 307050 0
02/10/2020
Approval date [1] 307050 0
28/10/2020
Ethics approval number [1] 307050 0

Summary
Brief summary
Trial website
Trial related presentations / publications
Public notes

Contacts
Principal investigator
Name 105850 0
A/Prof Laurence Weinberg
Address 105850 0
145 Studley Road, Heidelberg , VIC, 3084, Department of Anaesthesia, Austin Health
Country 105850 0
Australia
Phone 105850 0
+61 3 94963800
Fax 105850 0
Email 105850 0
[email protected]
Contact person for public queries
Name 105851 0
Laurence Weinberg
Address 105851 0
145 Studley Road, Heidelberg , VIC, 3084, Department of Anaesthesia, Austin Health
Country 105851 0
Australia
Phone 105851 0
+61 3 94963800
Fax 105851 0
Email 105851 0
[email protected]
Contact person for scientific queries
Name 105852 0
Laurence Weinberg
Address 105852 0
145 Studley Road, Heidelberg , VIC, 3084, Department of Anaesthesia, Austin Health
Country 105852 0
Australia
Phone 105852 0
+61 3 94963800
Fax 105852 0
Email 105852 0
[email protected]

Data sharing statement
Will individual participant data (IPD) for this trial be available (including data dictionaries)?
No
No/undecided IPD sharing reason/comment
As this is a retrospective observational study, patients have not provided consent for their data to be shared.


What supporting documents are/will be available?

No Supporting Document Provided



Results publications and other study-related documents

Documents added manually
No documents have been uploaded by study researchers.

Documents added automatically
SourceTitleYear of PublicationDOI
EmbaseMEasuring the impact of Anesthetist-administered medications volumeS on intraoperative flUid balance duRing prolonged abdominal surgEry (MEASURE Study).2022https://dx.doi.org/10.23736/S0375-9393.22.15918-3
N.B. These documents automatically identified may not have been verified by the study sponsor.