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A real-world study of the clinical use of eravacycline

A real-world study of the clinical use of eravacycline

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2400083038
Enrollment
Unknown
Registered
2024-04-15
Start date
2024-04-20
Completion date
Unknown
Last updated
2024-04-22

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

Conditions

Bacterial Infection

Interventions

Elacycline treatment group:None

Sponsors

Huashan hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Receive at least 1 dose of eravacycline during hospitalization. 2. Age =18 at the time of signing the informed consent. 3. Voluntarily participate in the study and sign the informed consent. If the subject is unable to read and/or sign the informed consent due to incapacity or other reasons, his/her guardian shall represent the informed process and sign the informed consent.

Exclusion criteria

Exclusion criteria: 1. Enrolling in any other clinical trials, including non-interventional studies. 2. Incomplete or absent medical history.

Design outcomes

Primary

MeasureTime frame
clinical outcome(i.e. treatment success, treatment failure or uncertain outcome);Microbial outcome;

Secondary

MeasureTime frame
Adverse reactions and drug resistance during treatment;Hospitalization days;Hospitalization expenses;The recurrence rate of infection;

Countries

China

Contacts

Public ContactHuang haihui

Institute of Antibiotics Huashan Hospital, Fudan University,12 M. Wulumuqi Road,Shanghai 200040, China

huanghaihui@fudan.edu.cn+86 139 1668 5836

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026