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
- Frequency of drug level testing recommended [Baseline]
Indication of how many critically ill patients treated with beta-lactams should receive TDM.
- 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
- 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: