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Retrospective analysis of clinical study on the effect of acetylcysteine nebulization inhalation combined with piperacillin/tazobactam on immune function and inflammatory levels in patients with stroke-associated pneumonia

Retrospective analysis of clinical study on the effect of acetylcysteine nebulization inhalation combined with piperacillin/tazobactam on immune function and inflammatory levels in patients with stroke-associated pneumonia

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600125619
Enrollment
Unknown
Registered
2026-05-28
Start date
2026-06-01
Completion date
Unknown
Last updated
2026-06-01

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

Conditions

Stroke-associated pneumonia

Interventions

Combined group (acetylcysteine nebulized inhalation combined with piperacillin tazobactam):None

Sponsors

Yuebei People's Hospital Affiliated to Shantou University Medical College
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Conform to the diagnostic criteria of SAP; 2. Stroke patients who are not receiving mechanical ventilation, aged =18 years, and did not have pulmonary infection before stroke; 3. No history of using immunosuppressants, glucocorticoids, or other immunotherapy within 6 months prior to enrollment; 4. Anti-infective treatment using piperacillin/tazobactam.

Exclusion criteria

Exclusion criteria: 1. Combined with infections in other parts; 2. Previous history of resistance to piperacillin/tazobactam, or allergy to the drugs used in this study; 3. Comorbidities such as congenital structural abnormalities of the respiratory system, chest trauma, chronic obstructive pulmonary disease, spontaneous pneumothorax, bronchial asthma, or other respiratory diseases, or comorbid chronic respiratory failure; 4. Combined pregnancy, severe endocrine and metabolic disorders, hematological diseases, or cardiac, hepatic, and renal dysfunction.

Design outcomes

Primary

MeasureTime frame
Levels of CD3+, CD4+, and CD8+ T lymphocytes;The levels of inflammatory marker (PCT, CRP, IL-6);

Secondary

MeasureTime frame
Duration of hospitalization;Adverse reaction;

Countries

China

Contacts

Public ContactYu Hongying

Yuebei People's Hospital Affiliated to Shantou University Medical College

297115458@qq.com+86 751 6913465

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Jun 11, 2026