Health Condition 1: C00-D49- Neoplasms
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Adults aged more than or equal to 18 years Histologically confirmed solid organ malignancy Planned to receive cisplatinbased chemotherapy for the first time in the current treatment course
Exclusion criteria
Exclusion criteria: Patients on maintenance dialysis before initiation of cisplatin Previous exposure to cisplatin within the past 12 months Pregnant or lactating women Inability or unwillingness to comply with protocol-mandated follow up
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To determine the incidence and severity of acute kidney injury in adults receiving cisplatin-based chemotherapy for solid organ malignanciesTimepoint: 6 months from recruitment | — |
Secondary
| Measure | Time frame |
|---|---|
| To identify clinical, biochemical, and treatment-related factors independently associated with the development of acute kidney injury following cisplatin-based chemotherapy. Timepoint: 6 months from recruitment;To evaluate changes in renal function, measured by estimated glomerular filtration rate (eGFR), from baseline to 6 months following initiation of cisplatin therapy. Timepoint: 6 months from recruitment;To document short-term clinical outcomes including requirement for renal replacement therapy (RRT), unplanned hospitalisations, mortality, and chemotherapy dose modification or discontinuation within 6 months of cisplatin initiation. Timepoint: 6 months from recruitment;To compare the predictive performance of CKD-EPI, MDRD, and Cockcroft Gault equations in identifying the risk of AKI associated with cisplatin-based chemotherapy. Timepoint: 6 months from recruitment | — |
Countries
India
Contacts
Department of Nephrology, Kasturba Hospital, Manipal.