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Renal Toxicity clinical trials

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NCT ID: NCT03316417 Completed - Adverse Effect Clinical Trials

Study of Adverse Renal Effects of Immune Checkpoints Inhibitors

ImmuNoTox(INT)
Start date: October 27, 2017
Phase:
Study type: Observational

Renal toxic events related to Immune Checkpoints Inhibitors therapy (Nivolumab, Pembrolizumab, Atezolizumab and Ipilimumab) have been recently reported. These were immune-allergic acute interstitial nephritis. However, no systematic study has ever focused on renal adverse effects. The investigators study here the evolution of renal function and the occurrence of nephrological events in a large monocentric cohort of patients treated with Immune Checkpoints Inhibitors in the Centre Hospitalier Lyon Sud. Nephrological parameters based on Serum Creatinine (SCr), estimate Glomerular Filtration Rate (eGFR) and urinary sediment are monitored. The aim of the study is to determine the incidence of renal events due to Immune Checkpoint Inhibitor treatment, particularly Acute Kidney Injury, (AKI) and identify the clinical presentation, histological description and risk factors.

NCT ID: NCT02116751 Completed - Renal Toxicity Clinical Trials

Frequency and Clinical Significance of Renal and Bone Toxicity in HIV-infected Patients

ComorVIH
Start date: April 2014
Phase: N/A
Study type: Observational

The purpose of this study is to determine the frequency of renal and bone toxicity in HIV infected patients receiving antiretroviral therapy, and the outcome in terms of treatment change or/and virological failure, in relation with the presence of classical factors, such as diabetes or hypertension, the role of HIV itself, because of chronic inflammation, and the effects of antiretroviral medication.

NCT ID: NCT00993135 Completed - Leukemia Clinical Trials

Kidney Dysfunction in Children and Young Adults Who Have Received Methotrexate for Acute Lymphoblastic Leukemia

Start date: December 2008
Phase: N/A
Study type: Observational

RATIONALE: Gathering information about how often kidney dysfunction occurs in children and young adults receiving methotrexate for acute lymphoblastic leukemia may help doctors learn more about the disease and plan the best treatment. PURPOSE: This research study is looking at kidney dysfunction in children and young adults who have received low-dose or intermediate-dose methotrexate for acute lymphoblastic leukemia.

NCT ID: NCT00834496 Withdrawn - Neurotoxicity Clinical Trials

Switching From One Type of Anti-rejection Drug (Tacrolimus or Cyclosporine) to Another (Sirolimus) Approximately 90-180 Days After Liver Transplantation

Start date: January 2009
Phase: N/A
Study type: Observational

Sirolimus can be safely switched as early as 90 days after liver transplantation with excellent tolerability and amelioration of the calcineurin inhibitor toxicity that initiated the switch.

NCT ID: NCT00695032 Suspended - Clinical trials for Unspecified Adult Solid Tumor, Protocol Specific

Kidney Damage in Patients Receiving Cisplatin and Ifosfamide for Solid Tumors

Start date: October 2007
Phase: N/A
Study type: Interventional

RATIONALE: Studying samples of blood and urine from patients with cancer in the laboratory may help doctors learn more about changes that occur in DNA and identify biomarkers related to cancer. It may also help doctors predict how patients will respond to treatment. PURPOSE: This research study is evaluating kidney damage in patients receiving cisplatin and ifosfamide for solid tumors.