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Nephrotoxicity clinical trials

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NCT ID: NCT06153147 Recruiting - Hypertension Clinical Trials

KIdney aNd blooD prESsure ouTcomes in Childhood Cancer Survivors (CCS)

KINDEST-CCS
Start date: January 5, 2024
Phase:
Study type: Observational

Background: Childhood cancer survivors (CCS) are at elevated risk of chronic health conditions. Chemotherapies can cause recurrent acute kidney injury which may progress to kidney fibrosis, chronic kidney disease (CKD) or hypertension (HTN). CCS surviving to adulthood are at ≥3 times the risk (vs. non-CCS) for CKD, HTN and lower quality of life. However, the timing of CKD and HTN onset in CCS completing cancer therapy in childhood remains unclear. Guidelines provide recommendations on managing post-cancer therapy effects in CCS, but they lack specificity on kidney testing content, frequency and complications. This discord is largely due to knowledge gaps on which CCS develop CKD or HTN after cancer therapy, when outcomes occur and their severity. Existing work has shown in select patients, CKD and HTN in CCS likely begins in the first 5 years post-cancer therapy and that the burden is significant. With robust data on CKD and HTN, international CCS follow-up guidelines can be optimized to include detailed and actionable recommendations on kidney and blood pressure monitoring and treatment.

NCT ID: NCT05673824 Recruiting - Nephrotoxicity Clinical Trials

Effect of Huaier Granule on Nephrotoxicity Associated With Targeted Therapy for Advanced Hepatobiliary Malignancies.

Start date: February 7, 2023
Phase: Phase 4
Study type: Interventional

This is a prospective, single-arm, single-center, exploratory study. The purpose of this study is to explore the effect of Huaier Granule on nephrotoxicity associated with anti-angiogenesis targeted therapy for advanced hepatobiliary malignancies.

NCT ID: NCT03817970 Recruiting - Nephrotoxicity Clinical Trials

Cisplatin Disposition and Kidney Injury

Start date: November 15, 2019
Phase: Phase 3
Study type: Interventional

This study is being done to determine 1) whether drugs to treat cisplatin-related nausea can influence harm to the kidneys, 2) whether cisplatin levels in the body can influence the risk of harm to the kidneys, and 3) whether a person's genetic make-up can increase or decrease the likelihood of kidney injury due to cisplatin therapy.

NCT ID: NCT03480971 Recruiting - Mucositis Clinical Trials

Treatment of Radiation and Cisplatin Induced Toxicities With Tempol

Start date: May 13, 2019
Phase: Phase 2
Study type: Interventional

A 10 week trial to assess the ability of Tempol to prevent and/or reduce toxicities associated with cisplatin and radiation treatment in head and neck cancer patients. Over the course of the 10 week trial, mucositis, nephrotoxicity, and ototoxicity will be monitored and assessed.

NCT ID: NCT02528448 Recruiting - Nephrotoxicity Clinical Trials

0,9% NaCl Effect on Kidney Function and Glycocalyx in Patients Operated on for Primary Hiparthrosis

KIPA
Start date: March 2015
Phase: Phase 4
Study type: Interventional

The purpose of this study is to determine if chloride is nephrotoxic using 0,9% saline versus Plasma-Lytein in patients having primary hip replacement surgery. The outcome is found measuring bio markers, vasoactive hormones and salt regulation. And to measure syndecan as a marker for glycocalyx degradation.

NCT ID: NCT01624324 Recruiting - Ototoxicity Clinical Trials

Aminoglycoside Plasma Level Measurement in Neonates With Infection

Start date: November 2010
Phase: N/A
Study type: Observational

The aim of this study is to determine whether the plasma concentration of aminoglycoside in Indonesia neonates with infection are within safe and effective range and its association with cochlear toxicity and nephrotoxicity.