Skip to content

Study on Precision Dosing Strategies of Anti-infective Agents in the Very Early Stage of Kidney Transplantation

Study on Precision Dosing Strategies of Anti-infective Agents in the Very Early Stage of Kidney Transplantation

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600128745
Enrollment
Unknown
Registered
2026-07-24
Start date
2026-08-01
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

None

Interventions

Kidney transplant very early anti-infection treatment observation group:None

Sponsors

Zhongnan Hospital of Wuhan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1.Aged >= 18 years old; 2.Patients receiving kidney transplantation within 0–5 days postoperatively; 3.Clinically planned administration of anti-infective agents for perioperative prophylaxis, empirical therapy or confirmed infection treatment, with an anticipated treatment duration of no less than 5 days; 4.Written informed consent obtained from the subject or legal surrogate; 5.Indwelling urinary catheter retained for at least 48 hours postoperatively to facilitate early urine sample collection; 6.Patients anticipated to be free of dialysis requirement with urine output or early graft functional recovery at enrollment.

Exclusion criteria

Exclusion criteria: 1.Previous kidney transplantation or combined multi-organ transplantation; 2.Patients requiring continuous renal replacement therapy in the early postoperative period; 3.Severe hepatic dysfunction, defined as Child-Pugh class C, or ALT/AST > 5 times the upper limit of normal accompanied by markedly elevated bilirubin; 4.Early postoperative use of ECMO, plasmapheresis or other extracorporeal therapies that substantially alter drug clearance; 5.Pregnancy or lactation; 6.Subjects judged inappropriate for enrollment by investigators, including those with unfeasible sampling, extremely short expected survival, severe missing clinical data, etc.

Design outcomes

Primary

MeasureTime frame
In vivo exposure of anti-infective agents;

Secondary

MeasureTime frame
Conventional renal function markers (Scr, eGFR);

Countries

China

Contacts

Public ContactLing Li

Zhongnan Hospital of Wuhan University

liling.12345@126.com+86 27 6781 2506

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Aug 10, 2026