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An International Survey on Aminoglycoside Practices in Critically Ill Patients: AMINO III Survey

An International Survey on Aminoglycoside Practices in Critically Ill Patients: AMINO III Survey

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02850029
Enrollment
964
Registered
2016-07-29
Start date
2016-05-21
Completion date
2017-12-31
Last updated
2025-11-21

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Critical Illness, Underdosing of Aminoglycosides

Keywords

antimicrobial, intensive care units

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.

Detailed description

Aminoglycosides are commonly used antibiotics for difficult to treat infections. However, aminoglycoside administration varies widely among countries. The aim of this multicenter observational study is to provide up-to-date and comprehensive descriptive data on current aminoglycoside (tobramycin, amikacin or gentamicin) use in a large cohort of critically ill patients in different countries. The benefits expected from this study are a better understanding of worldwide aminoglycoside prescription variability in critically ill patients and to determine the risk factors of inadequate aminoglycoside dosing regimens.

Interventions

Sponsors

Centre Hospitalier Universitaire de Nīmes
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

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

Exclusion criteria

* Aged \< 18 years of age * Previous inclusion in the study

Design outcomes

Primary

MeasureTime frame
Aminoglycoside current practices descriptive data in intensive care unitsSeven first days of aminoglycoside therapy

Secondary

MeasureTime frame
Aminoglycoside dosing regimensSeven first days of aminoglycoside therapy
Aminoglycoside therapy durationSeven first days of aminoglycoside therapy
Aminoglycoside therapeutic drug monitoringSeven first days of aminoglycoside therapy

Countries

Australia, Chile, France, Greece, United Kingdom

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 23, 2026