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Kidney Transplantation clinical trials

View clinical trials related to Kidney Transplantation.

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NCT ID: NCT02417870 Terminated - Clinical trials for Kidney Transplantation

Ultra-low Dose Subcutaneous IL-2 in Renal Transplantation

Start date: September 2015
Phase: Phase 1/Phase 2
Study type: Interventional

To investigate the safety and tolerability of treatment with low dose rIL-2 in renal transplant recipients. To assess the immunologic impact of low dose rIL-2 in renal transplant recipients. To assess the efficacy of low dose rIL-2 in renal transplant recipients.

NCT ID: NCT02409901 Active, not recruiting - Kidney Transplant Clinical Trials

Effects of Personalized Physical Rehabilitation in Kidney Transplant Recipients

Start date: October 2014
Phase: N/A
Study type: Interventional

This randomized controlled trial (RCT) will examine the effect of a novel 12 month personalized exercise rehabilitation program compared to standard care following kidney transplantation. Return to work or find work rates, markers of subclinical atherosclerosis, functional capacity, body composition, quality of life, kidney function, and adherence to exercise will be measured. The investigators' primary hypothesis is that a 12 month exercise rehabilitation program will increase the return to work or find work rate in kidney transplant recipients. The investigators additionally hypothesize that a 12 month exercise rehabilitation program will prevent a decline in subclinical atherosclerosis, increase functional capacity, and increase lean muscle mass.

NCT ID: NCT02399462 Withdrawn - Clinical trials for Kidney Transplantation

Acthar for Treatment of Post-transplant FSGS

Start date: March 2021
Phase: Phase 4
Study type: Interventional

This is an open label safety and feasibility trial using Acthar® in addition to center-specific standard therapy including plasma exchange, for treatment of post transplant recurrent FSGS and post transplant recurrent idiopathic membranous nephropathy. Subjects will receive Acthar® 40 units subcutaneously (SC) twice weekly for two weeks then 80 units SC twice weekly for 24 weeks.

NCT ID: NCT02392312 Completed - Clinical trials for Kidney Transplant Recipients

Observational Study to Evaluate the Safety and Efficacy of ATG-F on Kidney Transplant Recipients

Start date: January 21, 2015
Phase:
Study type: Observational

A multicenter, prospective, observational study to evaluate the safety and efficacy of individual batches of ATG-F in kidney transplant recipients.

NCT ID: NCT02377791 Enrolling by invitation - Kidney Transplant Clinical Trials

Impact of CYP3A5 Gene Polymorphisms on Tacrolimus Concentrations and Outcomes in Thai Transplant Recipients

Start date: July 2014
Phase: N/A
Study type: Observational

Tacrolimus is a drug used commonly in kidney transplant patients to prevent graft rejection. Tacrolimus acts in a very narrow range in the blood for its optimum activity. If the levels are too high, there is a risk of kidney injury, whereas, if the levels are too low there is a higher risk of rejection and graft loss. Genetic differences in the gene coding for the enzyme cytochrome P450 (CYP3A5), which is responsible for breaking down active tacrolimus can contribute to variations in blood levels of tacrolimus among different individuals taking the same dose of the drug. Certain genetic types lead to low concentrations, whereas certain genetic types can lead to high levels. The proportion of individuals with different types of genetic variations differ among different ethnic populations. Limited data are available in Thai subjects or on the risk have having certain types of genetic variations on the risk of rejection. This study aims to compare the effects of different types of CYP3A5 gene variations on Tacrolimus drug levels and risk of acute rejection in Thais.

NCT ID: NCT02374736 Completed - Clinical trials for Kidney Transplantation

Effect of Privigen Against Graft Loss

InAuGuRAL
Start date: February 5, 2016
Phase: Phase 3
Study type: Interventional

The principal objective of this pilot study is to determine whether the progression of chronic antibody-mediated rejection (ABMR) could be minimized by the post-transplant administration of high dose of Intravenous Immunoglobulins (IVIg). We test the hypothesis that repetitive IVIg administration reduces or stabilize the progressive loss of transplant function and the evolution to chronic ABMR in stable kidney transplant patients with HLA-DSA developed post-transplantion (de novo HLA-DSA) and concomitant humoral graft injury.

NCT ID: NCT02351427 Recruiting - Clinical trials for Kidney Transplantation

Bortezomib With Steroid Pulse Therapy for Acute Cellular Rejection in Kidney Transplantation

Start date: February 2015
Phase: Phase 3
Study type: Interventional

The purpose of this study is to determine whether bortezomib is effective in the treatment of acute cellular rejection after kidney transplantation.

NCT ID: NCT02346968 Completed - Clinical trials for Kidney Transplantation

Evaluation of CAF22 After Renal Transplantation

Start date: October 8, 2014
Phase:
Study type: Observational

Established markers of kidney function, such as creatinine, have considerable limitations in the diagnosis of delayed graft function (DGF) after kidney transplantation (KT). Indeed, creatinine does not accurately reflect minor changes of renal function as its levels change only upon significant fluctuations of the latter. CAF22 is a molecule which arises from the degradation of a larger protein and it is proposed to be a reliable and more sensitive marker of renal function. This study aims to further clarify this issue by measuring blood and urine concentrations of CAF22 and comparing them with creatinine levels before and after KT. The main assumption is that blood CAF22 levels could serve as a more sensitive kidney function biomarker than creatinine post-KT to detect DGF.

NCT ID: NCT02345577 Terminated - Clinical trials for Kidney Transplantation

Whole-body Vibration Physiotherapy in Kidney Transplantation

Start date: December 16, 2014
Phase: N/A
Study type: Interventional

Kidney recipients loose significant amounts of muscle mass and skeleton minerals in the early post-transplantation period and suffer from increasing abnormalities of neuromuscular functions. Stochastic whole body vibration (WBV) therapy is a relatively new form of movement physiotherapy that is used for strength training. Various clinical studies have shown that in addition to muscle function, WBV also improved body balance and bone mineral density. To study the impact of stochastic WBV physiotherapy on musculoskeletal parameters after renal transplantation, kidney transplant recipients will be enrolled and undergo WBV. The investigators hypothesize that WBV physiotherapy improves both maximum muscle strength and muscular performance

NCT ID: NCT02322567 Completed - Clinical trials for Kidney Transplantation

Left Ventricular Diastolic Dysfunction in Kidney Recipients

Start date: January 2012
Phase: N/A
Study type: Observational

The purpose of this study is to examine the relationship between pre-operative LV diastolic function and post-operative complications and kidney function in living-donor kidney transplantation patients.