Skip to content

Clinical effectiveness of aztreonam–avibactam: a retrospective multicenter cohort study

Clinical effectiveness of aztreonam–avibactam: a retrospective multicenter cohort study - ATMAVI

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
DRKS
Registry ID
DRKS00038893
Enrollment
15
Registered
2026-01-13
Start date
2026-02-01
Completion date
Unknown
Last updated
2026-03-30

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

Conditions

Severe bacterial infections in adult hospitalized patients, including severe pneumonia (e.g., hospital-acquired or ventilator-associated pneumonia) and complicated intra-abdominal infections, treated with aztreonam–avibactam in routine clinical care, particularly in the context of multidrug-resistant Gram-negative pathogens.

Interventions

Group 1: Single-arm retrospective cohort: All adult hospitalized patients treated with aztreonam–avibactam in routine clinical care (e.g., severe pneumonia or complicated intra-abdominal infection).

Sponsors

Charité – Universitätsmedizin Berlin, Klinik für Anästhesiologie und Intensivmedizin
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Adult hospitalized patients (=18 years) treated with aztreonam–avibactam in routine clinical care for at least 72 hours.

Exclusion criteria

Exclusion criteria: None.

Design outcomes

Primary

MeasureTime frame
Clinical treatment success with aztreonam–avibactam (improvement or resolution of infection-related symptoms at end of therapy or hospital discharge).

Secondary

MeasureTime frame
Microbiological clearance (negative cultures after end of therapy), safety/tolerability (adverse events, treatment discontinuation), 30-/60-day mortality, ICU and hospital length of stay.

Countries

Germany

Contacts

Public ContactOliver Hölsken

Charité – Universitätsmedizin Berlin, Klinik für Anästhesiologie und Intensivmedizin

oliver.hoelsken@charite.de+49 30 450 651 743

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Apr 4, 2026