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The Effect of Early Switching From Intravenous to Oral Antibiotics Therapy

The Effect of Early Switching From Intravenous to Oral Antibiotics Therapy: a Randomized Control Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04781439
Enrollment
210
Registered
2021-03-04
Start date
2020-03-01
Completion date
2020-09-29
Last updated
2021-03-04

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

Conditions

Skin and Subcutaneous Tissue Infection

Keywords

effectiveness, antibiotics

Brief summary

To date, many studies showed the great benefits of switching from IV to PO antibiotics in some infectious diseases, especially skin and soft tissue, urinary tract, respiratory tract, gallbladder, and biliary tract infection. Higher level of evidence is necessary to confirm the benefit of early switching protocol in infectious condition management. Therefore, we conducted a clinical trial to investigate the effectiveness and cost of IV-to-PO antibiotic switch therapy in some surgical infection conditions.

Detailed description

Introduction: The benefit of early switching from intravenous (IV) to oral (PO)was raising from the last decade. This randomized clinical trial was to evaluate the effect of early switching from IV to PO antibiotics on the outcome of surgical patients at a public hospital. Methods: Patients admitted for a therapeutic antibiotic to orthopedic and general surgery conditions were randomly assigned to three groups: control (non-switching), early switching (within 48-72 hours), and late switching (after 72 hours). The rate of effectiveness of each arm, length of hospital stay, length of IV antibiotics, and cost were recorded prospectively.

Interventions

PROCEDUREIV-to-PO conversion of antibiotics

IV-to-PO switching of antibiotics treatment

Sponsors

Gia Dinh People Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Investigator)

Eligibility

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

Inclusion criteria

* on the second day of IV antibiotic * no difficulties on taking oral medication * clinical improvement

Exclusion criteria

* n/a

Design outcomes

Primary

MeasureTime frameDescription
rate of effectiveness3 monthsrate of effectiveness of the infection treatment

Secondary

MeasureTime frameDescription
length of hospital stay3 monthslength of hospital stay after starting the antibiotic treatment
length of IV antibiotics3 monthslength of IV antibiotics usage
cost of treatment3 monthscost of antibiotics

Countries

Vietnam

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026