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Safety Study of Moxifloxacin in Children

Safety Study of Moxifloxacin in Children

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2200066109
Enrollment
Unknown
Registered
2022-11-24
Start date
2022-12-01
Completion date
Unknown
Last updated
2023-05-15

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

Conditions

atypical pathogens, resistant gram-negative bacteria, tuberculosis infection

Interventions

Quinolone treatment group:N/A
Non quinolone drug treatment group:N/A

Sponsors

Pediatric Intensive Care Unit, Beijing Children's Hospital, Capital Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
No minimum to 18 Years

Inclusion criteria

Inclusion criteria: 1. Children with 29d-18y atypical pathogens, drug-resistant Gram-negative bacteria and tuberculosis infection who were intravenously or orally administered with quinolones (ciprofloxacin 10 mg/kg/d, Q8h; levofloxacin 10 mg/kg/d, QD, maximum 14 days, maximum dose no more than 500 mg; moxifloxacin 10 mg/kg/d, QD, maximum 14 days, maximum dose no more than 400 mg) in the Department of Intensive Care Medicine and the Department of Respiratory Medicine II of Beijing Children's Hospital; 2. Administration time >= 3 days; 3. Signing the informed consent for off-label use.

Exclusion criteria

Exclusion criteria: no

Design outcomes

Primary

MeasureTime frame
X-ray of both knees;electrocardiogram;echocardiography;blood concentration;blood concentration;

Countries

China

Contacts

Public ContactQian Suyun

Pediatric Intensive Care Unit, Beijing Children's Hospital, Capital Medical University

syqian2020@163.com+86 13370115029

Outcome results

None listed

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