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Study on the Pharmaceutical Care Effectiveness of Clinical Pharmacists in Managing the Risk of Acute Kidney Injury Associated with the Combination of Vancomycin and Piperacillin-Tazobactam

Study on the Pharmaceutical Care Effectiveness of Clinical Pharmacists in Managing the Risk of Acute Kidney Injury Associated with the Combination of Vancomycin and Piperacillin-Tazobactam

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500115486
Enrollment
Unknown
Registered
2025-12-26
Start date
2026-01-01
Completion date
Unknown
Last updated
2026-01-05

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

Conditions

Infectious disease

Interventions

Pharmaceutical care group:From January to December 2026, pharmacists will closely monitor patients who meet the inclusion and exclusion criteria. Based on conventional therapy, clinical pharmacists ma
timely culture specimens are ensured for patients on VPT combination therapy. Daily assessments of antimicrobial efficacy are performed, and de-escalation or switching to targeted agents is implemente
Historical contr

Sponsors

Nanjing Drum Tower Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Patients aged 18–80 years who received the VPT regimen for at least 48 h at the participating centers; 2. Expected survival > 72 h; 3. Signed informed consent.

Exclusion criteria

Exclusion criteria: 1. Receipt of two or more ß-lactam agents during the concomitant period; 2. Patients on extracorporeal membrane oxygenation (ECMO); 3. Death within 48 h after initiation of combination antibiotic therapy; 4. Presence of shock or already-established AKI between hospital admission and the start of the target antimicrobial regimen; 5. Obstructive uropathy such as nephrolithiasis; 6. Use of intravenous polymyxins or aminoglycosides during the study follow-up; 7. Creatinine clearance < 30 mL/min; 8. Pregnant patients.

Design outcomes

Primary

MeasureTime frame
Drug-related AKI;

Secondary

MeasureTime frame
Severe DRAKI;Any AKI;No-AKI 30 day survival;Clinical cure;

Countries

China

Contacts

Public ContactChen Dayu

Nanjing Drum Tower Hospital

cdy_pharmacy@njglyy.com+86 25 8310 6666

Outcome results

None listed

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