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Trial details imported from ClinicalTrials.gov
For full trial details, please see the original record at
https://clinicaltrials.gov/study/NCT02850029
Registration number
NCT02850029
Ethics application status
Date submitted
27/07/2016
Date registered
29/07/2016
Titles & IDs
Public title
An International Survey on Aminoglycoside Practices in Critically Ill Patients: AMINO III Survey
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Scientific title
An International Survey on Aminoglycoside Practices in Critically Ill Patients: AMINO III Survey
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Secondary ID [1]
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IRB 15 04 08
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Universal Trial Number (UTN)
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Trial acronym
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Linked study record
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Health condition
Health condition(s) or problem(s) studied:
Underdosing of Aminoglycosides
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Critical Illness
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Condition category
Condition code
Intervention/exposure
Study type
Observational
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Patient registry
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Target follow-up duration
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Target follow-up type
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Description of intervention(s) / exposure
critically ill patients - Critically ill patients admitted in intensive care units and receiving one of the following aminoglycosides: gentamicin, tobramycin and amikacin as part of their usual care.
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Comparator / control treatment
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Control group
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Outcomes
Primary outcome [1]
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Aminoglycoside current practices descriptive data in intensive care units
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Assessment method [1]
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Timepoint [1]
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Seven first days of aminoglycoside therapy
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Secondary outcome [1]
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Aminoglycoside dosing regimens
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Assessment method [1]
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Timepoint [1]
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Seven first days of aminoglycoside therapy
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Secondary outcome [2]
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Aminoglycoside therapy duration
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Assessment method [2]
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Timepoint [2]
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Seven first days of aminoglycoside therapy
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Secondary outcome [3]
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Aminoglycoside therapeutic drug monitoring
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Assessment method [3]
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Timepoint [3]
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Seven first days of aminoglycoside therapy
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Eligibility
Key inclusion criteria
* Age = 18 years old
* Intensive care unit patients
* Receiving aminoglycoside therapy for a sepsis according to the Third International Consensus Definitions for Sepsis and Septic Shock
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Minimum age
18
Years
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Maximum age
No limit
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Sex
Both males and females
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Can healthy volunteers participate?
No
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Key exclusion criteria
* Aged < 18 years of age
* Previous inclusion in the study
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Study design
Purpose
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Duration
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Selection
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Timing
Prospective
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Statistical methods / analysis
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Recruitment
Recruitment status
Completed
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Data analysis
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Reason for early stopping/withdrawal
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Other reasons
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Date of first participant enrolment
Anticipated
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Actual
21/05/2016
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Date of last participant enrolment
Anticipated
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Actual
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Date of last data collection
Anticipated
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Actual
31/12/2017
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Sample size
Target
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Accrual to date
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Final
964
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Recruitment in Australia
Recruitment state(s)
QLD
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Recruitment hospital [1]
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Royal Brisbane Women's Hospital - Brisbane
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Recruitment hospital [2]
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Royal Brisbane and Women's Hospital - Brisbane
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Recruitment hospital [3]
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Frankston Hospital Victoria - Frankston
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Recruitment hospital [4]
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Sunshine Coast hospital - Sunshine Coast
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Recruitment hospital [5]
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Toowoomba Hospital - Toowoomba
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Recruitment postcode(s) [1]
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4029 - Brisbane
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Recruitment postcode(s) [2]
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- Brisbane
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Recruitment postcode(s) [3]
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- Frankston
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Recruitment postcode(s) [4]
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- Sunshine Coast
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Recruitment postcode(s) [5]
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- Toowoomba
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Recruitment outside Australia
Country [1]
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Chile
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State/province [1]
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Region DE LOS RIOS
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Country [2]
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Chile
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State/province [2]
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Santiago
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Country [3]
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France
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State/province [3]
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Paca
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Country [4]
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France
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State/province [4]
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Aix-en-provence
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Country [5]
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France
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State/province [5]
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Ales
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Country [6]
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France
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State/province [6]
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Amiens
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Country [7]
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France
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State/province [7]
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Angers
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France
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Arles
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France
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Aulnay-sous-Bois
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France
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Aurillac
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Avignon
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Besançon
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Bordeaux
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France
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Boulogne sur mer
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France
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Brest
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Caen
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Maubeuge
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Morlaix
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Nancy
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Nantes
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Nice
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Nimes
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Paris
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PAU
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Poitiers
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Rennes
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Roanne
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Rodez
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Rouen
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Saint Brieuc
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Saint Denis
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Saint-etienne
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Salon de Provence
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Ioánnina
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Greece
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Thessaloníki
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United Kingdom
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Birmingham
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Oxford
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Prescot
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Sheffield
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United Kingdom
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Southampton
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Funding & Sponsors
Primary sponsor type
Other
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Name
Centre Hospitalier Universitaire de Nimes
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Address
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Country
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Ethics approval
Ethics application status
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Summary
Brief summary
This is an international observational cohort study on current aminoglycoside practices in intensive care units. Clinical and demographic data, dosing and therapeutic drug monitoring data will be collected during the first week of aminoglycoside (tobramycin, amikacin or gentamicin) administration in different countries over a year. A minimum of ten consecutive patients will be enrolled at each site.
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Trial website
https://clinicaltrials.gov/study/NCT02850029
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Trial related presentations / publications
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Public notes
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Contacts
Principal investigator
Name
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Claire Roger, MD
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Address
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Centre Hospitalier Universitaire de Nîmes
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Country
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Phone
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Fax
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Email
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Contact person for public queries
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Phone
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Fax
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Email
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Contact person for scientific queries
Data sharing statement
Will individual participant data (IPD) for this trial be available (including data dictionaries)?
No
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No/undecided IPD sharing reason/comment
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What supporting documents are/will be available?
No Supporting Document Provided
Results publications and other study-related documents
No documents have been uploaded by study researchers.
Results not provided in
https://clinicaltrials.gov/study/NCT02850029