Provider Perspectives on Beta-lactam Therapeutic Drug Monitoring Programs in the Critically Ill

Sponsor
Mayo Clinic (Other)
Overall Status
Active, not recruiting
CT.gov ID
NCT04755777
Collaborator
(none)
138
3
26.3
46
1.8

Study Details

Study Description

Brief 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.

Condition or Disease Intervention/Treatment Phase

    Study Design

    Study Type:
    Observational
    Anticipated Enrollment :
    138 participants
    Observational Model:
    Other
    Time Perspective:
    Cross-Sectional
    Official Title:
    Provider Perspectives on Beta-lactam Therapeutic Drug Monitoring Programs in the Critically Ill: a Multicenter Mixed-methods Study
    Actual Study Start Date :
    Oct 22, 2020
    Anticipated Primary Completion Date :
    Dec 31, 2022
    Anticipated Study Completion Date :
    Dec 31, 2022

    Outcome Measures

    Primary Outcome Measures

    1. Frequency of drug level testing recommended [Baseline]

      Indication of how many critically ill patients treated with beta-lactams should receive TDM.

    2. Nature of drug level testing recommended [Baseline]

      Indication of which types of critically ill patients treated with beta-lactams should receive TDM

    Secondary Outcome Measures

    1. Determinants of beta-lactam TDM implementation [Baseline]

      List of factors associated with successful beta-lactam TDM implementation

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    Yes
    Inclusion Criteria:
    • Providers involved with beta-lactam TDM for critically ill patients
    Exclusion Criteria:
    • None

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 UF Health Shands Gainesville Florida United States 32610
    2 Mayo Clinic Rochester Minnesota United States 55902
    3 Royal Brisbane and Women's Hospital Herston Queensland Australia 4029

    Sponsors and Collaborators

    • Mayo Clinic

    Investigators

    • Principal Investigator: Erin Barreto, Pharm. D.,R.Ph., Mayo Clinic

    Study Documents (Full-Text)

    None provided.

    More Information

    Additional Information:

    Publications

    None provided.
    Responsible Party:
    Erin Barreto, Principal Investigator, Mayo Clinic
    ClinicalTrials.gov Identifier:
    NCT04755777
    Other Study ID Numbers:
    • 20-007528
    First Posted:
    Feb 16, 2021
    Last Update Posted:
    Feb 16, 2022
    Last Verified:
    Feb 1, 2022
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Keywords provided by Erin Barreto, Principal Investigator, Mayo Clinic
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Feb 16, 2022