Clinical Trials Logo

Kidney Transplantation clinical trials

View clinical trials related to Kidney Transplantation.

Filter by:

NCT ID: NCT01872455 Completed - Clinical trials for Kidney Transplantation

Diet Rich in N-3 Polyunsaturated Fatty Acids in Renal Transplant Recipients

Start date: January 2010
Phase: Phase 4
Study type: Interventional

n-3 Polyunsaturated fatty acids (PUFAs) supplementation reduces systemic inflammation and improves renal and cardiovascular prognosis in kidney transplant recipients. A good patient compliance is often difficult to obtain because bad tasting fish oils are used as n-3 PUFA source. Therefore, we explored whether n-3 beneficial effects can be obtained by administering a diet based on n-3 rich foods.

NCT ID: NCT01871753 Completed - Clinical trials for Kidney Transplantation

The Bacteriuria in Renal Transplantation (BiRT) Study: A Trial Comparing Antibiotics Versus no Treatment in the Prevention of Symptomatic Urinary Tract Infection in Kidney Transplant Recipients With Asymptomatic Bacteriuria

BiRT
Start date: April 2014
Phase: Phase 4
Study type: Interventional

The purpose of this study is to compare antibiotics versus no-treatment in kidney transplant recipients with asymptomatic bacteriuria.

NCT ID: NCT01860820 Completed - Kidney Transplant Clinical Trials

The Effect of Neuromuscular Stimulation on Post-Transplant Leg Edema

Start date: June 2015
Phase: N/A
Study type: Interventional

This will be a randomized, controlled trial involving kidney and kidney pancreas transplant patients. There will be 2 groups and patients that will be randomized to one of the two groups. Clinical outcomes will be compared for those in each group and clinical differences between patients who receive routine medical therapy with IPC/TEDS versus the Geko device will also be evaluated.

NCT ID: NCT01860183 Completed - Clinical trials for Kidney Transplantation

Effect of 3g Versus 2 g MMF in Combination With Tacrolimus on Progression of Renal Allograft Interstitial Fibrosis

Start date: May 2013
Phase: Phase 4
Study type: Interventional

Development of chronic changes (scarring) in transplanted kidney tissue is a major cause of long-term kidney function deterioration and ultimately graft loss. It results from both immunologic and non-immunologic mechanisms. Mycophenolate mofetil (MMF) is immunosuppressive drug used for prevention of rejection after kidney transplant, usually in combination with a calcineurin inhibitor (tacrolimus or cyclosporine), with or without corticosteroids. Besides immunosuppression, MMF may also have direct antifibrotic properties. Tacrolimus has potent immunosuppressive effects and is the cornerstone of contemporary posttransplant immunosuppressive therapy in kidney recipients. However, it is also nephrotoxic. The hypothesis of the present study is that in the setting of similar net immunosuppression, higher dose of MMF (3 g daily) will result in slower progression of kidney fibrosis during first year posttransplant as compared to MMF 2 g daily. To test this hypothesis, the present study will randomly assign low immunological risk kidney transplant recipients to either 2g or 3 g MMF daily, in combination with tacrolimus, with, or without maintenance steroids. All patients will have kidney biopsy at implantation and at 12 months after transplantation. Main outcome will be 1-year change in chronic kidney histology (interstitial fibrosis) assessed by protocol biopsy.

NCT ID: NCT01855438 Completed - Clinical trials for Kidney Transplant Candidates

Increasing Communication About Live Donor Kidney Transplant

Start date: May 2013
Phase: N/A
Study type: Interventional

This study will test the efficacy of a communication intervention intended to increase and improve kidney transplant candidates' communication about live donor kidney transplantation.

NCT ID: NCT01842269 Completed - Clinical trials for Kidney Transplantation

Evaluate the Efficacy and Safety of My-Rept® Tablet vs. My-Rept® Capsule in Combination With Tacrolimus in Kidney Transplant Patients

My-Rept_KT_P4
Start date: January 2013
Phase: Phase 4
Study type: Interventional

Efficacy and Safety of My-Rept® Tablet(Mycophenolate Mofetil 500mg/Tab.) versus My-Rept® Capsule(Mycophenolate Mofetil 250mg/Cap.) in Combination with Tacrolimus in Kidney Transplant Patients

NCT ID: NCT01839929 Completed - Clinical trials for Kidney Transplantation

A Study to Assess the Safety and Efficacy of ADVAGRAF (Tacrolimus Modified Release Formulation) in Kidney Transplant Patients Who Were Treated With PROGRAF

PeACE
Start date: September 2010
Phase: Phase 4
Study type: Interventional

The purpose of this study is to evaluate the efficacy of tacrolimus modified release formulation Advagraf® after conversion from Prograf® in stable kidney transplant patients.

NCT ID: NCT01820572 Completed - Clinical trials for Kidney Transplantation

A Study in Maintenance Kidney Transplant Recipients Following Conversion to Nulojix® (Belatacept)-Based

Start date: March 27, 2013
Phase: Phase 3
Study type: Interventional

The primary purpose is to assess the benefits and risks of changing from Cyclosporine or Tacrolimus to Belatacept between 6-60 months after kidney transplant.

NCT ID: NCT01802268 Completed - Kidney Transplant Clinical Trials

Planned Conversion From TAC to SRL-based Regimen in de Novo Kidney Transplant Recipients

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

Background Early conversion from calcineurin inhibitor to mammalian target of rapamycin inhibitor is one of the immunosuppressive strategies that have been investigated to mitigate long-term CNi associated adverse events. This study aims to evaluate the conversion from tacrolimus to sirolimus in de novo kidney transplant recipients. This multicenter, open-label study, planned to enroll 297 patients initially treated with tacrolimus, enteric-coated mycophenolate sodium (1440 mg/day, orally) and prednisone. The primary objective is to show superior glomerular filtration rate in the SRL group at 24 months after transplantation.

NCT ID: NCT01800851 Completed - Diabetes Clinical Trials

Calorimetry, Insulin Resistance and Energy Metabolism Study to Understand the Risk of Obesity in Kidney Transplanted Patients

CALIMERO
Start date: January 2008
Phase: N/A
Study type: Interventional

Weight gain is a common complication after transplantation. It has adverse effects such as hypertension, dyslipidemia, and insulin resistance. Weight gain is implicated in the increased cardiovascular risk and the long-term loss of graft function. Weight loss achieved by a suitable dietary intervention in these patients transplanted kidney can correct lipid disorders and facilitate balance blood pressure. The identification of mechanisms responsible for weight gain would suggest prevention strategies and allow to align the caloric energy needs of renal transplant patients.