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Pharmacokinetics of Ceftriaxone Free Fraction

NCT05061875 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 20

Last updated 2021-11-17

No results posted yet for this study

Summary

Prospective observational follow-up study for the study and modeling of the pharmacokinetics of the free fraction of ceftriaxone in patients treated with high doses of ceftriaxone (greater than or equal to 4 grams per day).

Conditions

  • Ceftriaxone Poisoning

Sponsors & Collaborators

  • Fundación Pública Andaluza para la gestión de la Investigación en Sevilla

    lead OTHER

Principal Investigators

  • Maria Victoria Gil Navarro · Hospitales Universitarios Virgen del Rocío

Eligibility

Min Age
55 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2021-03-01
Primary Completion
2022-02-01
Completion
2022-02-01

Countries

  • Spain

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05061875 on ClinicalTrials.gov