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Pilot Study - Safety and Efficacy of Dalbavancin in Early Outpatient Treatment of Erysipelas and Limited Cellulitis

Status
Not yet recruiting
Phases
Phase 4
Study type
Interventional
Source
EU CTIS
Registry ID
CTIS2025-524877-18-00
Enrollment
50
Registered
2026-04-07
Start date
Unknown
Completion date
Unknown
Last updated
2026-04-07

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

Conditions

Acute bacterial skin and skin structure infection (ABSSSI) Erysipelas

Brief summary

Percentage of patients who are dischargeable 48-72 hours after the Dalbavancin infusion due to sufficient infection control., Incidence of adverse events during therapy (up to day 28)., Incidence of Dalbavancin-associated adverse events.

Detailed description

Proportion of patients who do not require readmission between hospital discharge and follow-up evaluation associated with infection., Percentage of inpatient patients who can be discharged on day 8 due to sufficient infection control, Proportion of patients who require readmission on day 8 due to insufficient infection control., Duration of hospitalization., Infection-associated rehospitalization rate within 4 weeks after discharge., Percentage of patients without recurrent BHWI within 4 weeks after discharge., Proportion of patients without recurrent BHWI within a 4-6 week follow-up period., Percentage of patients requiring a change in antibiotic therapy (regimen change) within 14 days of starting treatment., Proportion of patients with adequate antibiotic coverage by Dalbavancin according to the antibiogram.

Interventions

Sponsors

Gemeinnutzige Salzburger Landes kliniken Betriebsgesellschaft mbH
Lead SponsorOTHER

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Design outcomes

Primary

MeasureTime frame
Percentage of patients who are dischargeable 48-72 hours after the Dalbavancin infusion due to sufficient infection control., Incidence of adverse events during therapy (up to day 28)., Incidence of Dalbavancin-associated adverse events.

Secondary

MeasureTime frame
Proportion of patients who do not require readmission between hospital discharge and follow-up evaluation associated with infection., Percentage of inpatient patients who can be discharged on day 8 due to sufficient infection control, Proportion of patients who require readmission on day 8 due to insufficient infection control., Duration of hospitalization., Infection-associated rehospitalization rate within 4 weeks after discharge., Percentage of patients without recurrent BHWI within 4 weeks after discharge., Proportion of patients without recurrent BHWI within a 4-6 week follow-up period., Percentage of patients requiring a change in antibiotic therapy (regimen change) within 14 days of starting treatment., Proportion of patients with adequate antibiotic coverage by Dalbavancin according to the antibiogram.

Outcome results

None listed

Source: EU CTIS · Data processed: Apr 8, 2026