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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04755777
Other study ID # 20-007528
Secondary ID
Status Completed
Phase
First received
Last updated
Start date October 22, 2020
Est. completion date December 31, 2022

Study information

Verified date February 2023
Source Mayo Clinic
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The purpose of the study is to characterize various healthcare practitioners' perspectives on implementation of beta-lactam therapeutic drug monitoring in critical care practice.


Recruitment information / eligibility

Status Completed
Enrollment 138
Est. completion date December 31, 2022
Est. primary completion date December 31, 2022
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Providers involved with beta-lactam TDM for critically ill patients Exclusion Criteria: - None

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
Australia Royal Brisbane and Women's Hospital Herston Queensland
United States UF Health Shands Gainesville Florida
United States Mayo Clinic Rochester Minnesota

Sponsors (1)

Lead Sponsor Collaborator
Mayo Clinic

Countries where clinical trial is conducted

United States,  Australia, 

References & Publications (1)

Ausman S, Boehmer K, et al. Open Forum Infectious Diseases. 2022;9(Supplement 2):ofac492.034.

Outcome

Type Measure Description Time frame Safety issue
Primary Frequency of drug level testing recommended Indication of how many critically ill patients treated with beta-lactams should receive TDM. Baseline
Primary Nature of drug level testing recommended Indication of which types of critically ill patients treated with beta-lactams should receive TDM Baseline
Secondary Determinants of beta-lactam TDM implementation List of factors associated with successful beta-lactam TDM implementation Baseline
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