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Precise Medication Study of Ceftriaxone in Pediatric Community-Acquired Pneumonia Based on Evidence-based Medicine and Pulmonary PPK/PD Models

Precise Medication Study of Ceftriaxone in Pediatric Community-Acquired Pneumonia Based on Evidence-based Medicine and Pulmonary PPK-PD Models

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600121185
Enrollment
Unknown
Registered
2026-03-26
Start date
2026-04-01
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

Community Acquired Pneumonia

Interventions

PK/PD study section-Cefotaxime observation group:None
Real-world study section-Cefotaxime observation group:None

Sponsors

Qingdao Women and Children's Hospital?
Lead Sponsor

Eligibility

Sex/Gender
All
Age
No minimum to 18 Years

Inclusion criteria

Inclusion criteria: 1. Inclusion Criteria for the PK/PD Study Section (1) Children aged 0–18 years (2) Diagnosed with community-acquired pneumonia according to the Guidelines for the Management of Community-Acquired Pneumonia in Children (2024 Revision) (3) Treated with ceftriaxone for more than 2 days (4) Informed consent voluntarily signed by the children's guardians 2. Inclusion Criteria for the Real-World Study (1) Meet the diagnostic criteria of the Guidelines for the Management of Community-Acquired Pneumonia in Children (2024 Revision) (2) Age < 18 years (3) Require treatment with ceftriaxone (4) Informed consent voluntarily signed by the children's guardians

Exclusion criteria

Exclusion criteria: 1. Exclusion Criteria for the PK/PD Study Section (1) Patients allergic to ceftriaxone (2) Concurrent severe diseases, such as cardiovascular diseases, kidney diseases, liver diseases, hematological disorders, etc. (3) Patients currently participating in other clinical drug trials (4) Other conditions deemed unsuitable for inclusion in this study by the researchers, such as lack of accurate medication administration or blood sampling information 2. Exclusion Criteria for the Real-World Study (1) Allergy to ceftriaxone (2) Concurrent use of other antibacterial drugs (3) Patients with concurrent immunological diseases (4) Poor compliance or inability to follow the prescribed medication regimen for any reason (5) Patients with concurrent congenital diseases

Design outcomes

Primary

MeasureTime frame
blood drug concentration;Drug concentration in ELF;The efficacy rate of the optimized regimen of ceftriaxone;The time for improvement of clinical symptoms;Inflammation-related indicators: Whole blood white blood cell count (WBC), neutrophil percentage, C-reactive protein (CRP), procalcitonin (PCT), interleukin-6 (IL-6), lactate dehydrogenase (LDH), D-dimer (DD);

Countries

China

Contacts

Public ContactLiu Chang

Qingdao Women and Children's Hospital?

lch1001@yeah.net+86 185 5326 3607

Outcome results

None listed

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