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Renal Function clinical trials

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NCT ID: NCT01320722 Completed - Obesity Clinical Trials

Study of Vitamin D and Uric Acid Lowering on Kidney and Blood Vessel Function

MODERATE
Start date: March 2011
Phase: N/A
Study type: Interventional

The investigators hypothesize that, among non-hypertensive overweight and obese individuals, treatment of vitamin D deficiency and lowering uric acid concentrations (by either xanthine oxidase inhibition or increased renal excretion) will attenuate renin angiotensin system (RAS) activation, improve endothelial function, and lower blood pressure.

NCT ID: NCT01227213 Completed - Hypertension Clinical Trials

The Vascular and Metabolic Effects of Sunitinib in Patients With Metastatic Renal Cell Carcinoma

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

Rationale: The introduction of angiogenesis inhibitors, like sunitinib and bevacizumab, has improved the outcome of patients with several types of cancer remarkably. However, their application is hampered by side effects, such as development of hypertension with consequences for renal and cardiac function. Moreover patients treated with angiogenesis inhibitors may suffer from weight loss, and insulin sensitivity during treatment appears to change. The treatment with angiogenesis inhibitors, will improve life expectancy of patients with various cancer diagnoses and therefore the clinical relevance of both short term and long lasting adverse events will translate into reduced quality of life. In addition, premature withdrawal of angiogenesis inhibitors due to side effects may result in lower response, shorter duration of response and possibly a shorter survival. Therefore, adequate treatment of above mentioned side effects in patients treated with angiogenesis inhibitors is of relevance for the response rate, the duration of progression free survival and overall survival and for quality of life. Mechanistic insight in the pathogenesis of these side effects will help optimizing treatment. Objective: The primary objective of the study is to investigate the effect of sunitinib on endothelial function, insulin sensitivity, renal function and renal blood flow. Study design: Single-centre non randomized observational study Study population: 30 Patients (>18 years old) starting with sunitinib as treatment for metastatic renal cell carcinoma.

NCT ID: NCT01217736 Completed - Renal Function Clinical Trials

Direct Renin Inhibition and the Kidney

Start date: September 2010
Phase: Phase 1
Study type: Interventional

The objective of the study is to determine the magnitude of the effect of direct renin inhibition by VTP-27999 on renal plasma flow and kidney function.

NCT ID: NCT01138241 Completed - HIV Infection Clinical Trials

Tenofovir Renal Toxicity and Glomerular Filtration Rate (GFR) Validation

Start date: March 2010
Phase:
Study type: Observational

To assess and validate equation eGFR in HIV-infected subjects and -uninfected Thai patients

NCT ID: NCT00992043 Completed - Diabetes Clinical Trials

Creatine Supplementation and Diabetes

Start date: October 2009
Phase: N/A
Study type: Interventional

Creatine supplementation is capable of improving glucose tolerance in healthy subjects. The researchers aim to investigate whether this supplement can affect metabolic control in diabetic patients.

NCT ID: NCT00634920 Completed - Renal Function Clinical Trials

Evaluation of Early Conversion to Everolimus From Cyclosporine in de Novo Renal Transplant Recipients

Start date: March 2008
Phase: Phase 4
Study type: Interventional

This study is designed to evaluate if early conversion to everolimus from cyclosporine in de novo renal transplant recipients can improve long-term renal function and slow down the progression of chronic allograft nephropathy

NCT ID: NCT00586118 Completed - Renal Function Clinical Trials

Inhalative Sedation in ICU With Sevoflurane Via Anaesthetic Conserving Device Compared to Propofol

Start date: December 2006
Phase: N/A
Study type: Observational

The evaluation of the presented study will work on the practicability of inhalative sedation on the ICU, potential benefits and limitations of the ACD system in a postoperative sedated patient population in comparison to a standard intravenous sedation regimen with propofol, and focus on renal and hepatic function, cardioprotection and pharmacoeconomics

NCT ID: NCT00117390 Completed - Critical Illness Clinical Trials

Evaluation of the Optimal Technique for Determination of Renal Function of Critically Ill Patients

Start date: June 2004
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate the optimal technique for determination of the renal function of critically ill patients.