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Clinical Efficacy Observation of Intravenous Cefotaxime Sodium and Tazobactam Sodium in the Treatment of Moderate to Severe Pulmonary Infection

Clinical Efficacy Observation of Intravenous Cefotaxime Sodium and Tazobactam Sodium in the Treatment of Moderate to Severe Pulmonary Infection

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500102245
Enrollment
Unknown
Registered
2025-05-12
Start date
2025-05-19
Completion date
Unknown
Last updated
2025-05-19

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

Conditions

Moderate to severe lung infection

Interventions

Experimental group:Cefotaxime sodium and tazobactam sodium for injection, intravenous drip. 2.34 g/time, q8h. Course of treatment: 7 days (the course of treatment depends on the course of the disease

Sponsors

Jiangsu Shengze Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: Participants must meet all the following criteria to be included in this study: 1) meet the diagnostic criteria in the "Guidelines for the Diagnosis and Treatment of Community-Acquired Pneumonia in Adults in China (2016 Edition)"; 2) CAP severity: CURB-65 score of 2-3; 3) Age: 18-74 years, gender not specified; 4) Voluntarily sign the informed consent form.

Exclusion criteria

Exclusion criteria: Patients who meet any of the following criteria will be excluded from this study: 1) do not meet the above diagnostic criteria and inclusion criteria; 2) Patients with secondary pancreatitis caused by tumors or autoimmune diseases; 3) Primary diseases or malignant tumors of the heart, liver, lung, kidney, blood and other systems that are serious and can endanger life; 4) Patients with liver disease, ALT or AST greater than 2 times the upper limit of normal or TBIL greater than 2 times upper limit of normal (excluding patients with normal transaminase but abnormal TBIL); Patients with renal insufficiency, serum creatinine and blood urea nitrogen greater than 1.5 times the upper limit of the normal value; 5) There are people who have a clear allergy to the components of known experimental drugs; 6) Those with a history of alcohol or drug abuse. Patients with poor compliance; 7) Those with mental illness or who are uncooperative.

Design outcomes

Primary

MeasureTime frame
Bacteriology efficacy;Blood routine;C-reactive protein ;Clinical recovery rate after 7 days of treatment;

Countries

China

Contacts

Public ContactYu Lu

Jiangsu Shengze Hospital

uuszluyu@sina.com+86 512 6309 7031

Outcome results

None listed

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