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COMPLETED
NCT07874373
NA

Magnesium Supplementation for the Prevention of Cisplatin-Induced Nephrotoxicity

Sponsor: Grigore T. Popa University of Medicine and Pharmacy

View on ClinicalTrials.gov

Summary

This prospective, randomized, open-label study evaluated whether intravenous magnesium sulphate added to standard hydration could reduce cisplatin-associated renal toxicity in adult patients with solid tumors receiving weekly cisplatin-based chemoradiotherapy. Participants were assigned to standard hydration with intravenous saline and furosemide or to the same hydration protocol supplemented with 1 g of intravenous magnesium sulphate before cisplatin administration. The primary outcome was early renal toxicity assessed 48 hours after cisplatin administration. Secondary outcomes included renal dysfunction at one year, changes in urinary kidney injury biomarkers (KIM-1, NGAL, and suPAR), hematological toxicity, and treatment response

Official title: Prevention of Cisplatin Nephrotoxicity in Cancer Patients

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

INTERVENTIONAL

Enrollment

43

Start Date

2021-03-01

Completion Date

2024-12-31

Last Updated

2026-10-14

Healthy Volunteers

No

Interventions

DRUG

Magnesium sulphate

1 g intravenously before cisplatin administration, administered with the pre-hydration regimen.

DRUG

Furosemide

20 mg intravenously before cisplatin administration as part of the hydration protocol.

DRUG

Saline (0.9% NaCl)

1 L of 0.9% sodium chloride before cisplatin and 1 L after cisplatin.

Locations (1)

Grigore T Popa University of Medicine and Pharmacy Iasi

Iași, Romania