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Kidney Transplantation clinical trials

View clinical trials related to Kidney Transplantation.

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NCT ID: NCT02282124 Completed - Clinical trials for Kidney Transplantation

Effectiveness of an APN-led Self-management Program in Patients in the First Year After Renal Transplantation

SMP-NEP
Start date: May 2012
Phase: N/A
Study type: Interventional

The aim of this study is to investigate the effectiveness of the program in patients after renal transplantation using a randomized controlled trial design. Physical, behavioural, and clinical outcomes will be measured at baseline before randomization then 8 and 12 months later.

NCT ID: NCT02268201 Terminated - Clinical trials for Kidney Transplant Recipients

A Study to Evaluate the Efficacy and Safety in Kidney Transplant Recipients When Changed From Cyclosporine to Tacrolimus Prolonged-release Capsule or Tacrolimus Capsule

Start date: July 23, 2013
Phase: Phase 4
Study type: Interventional

KTx recipients receiving cyclosporine-based immunosuppressive therapy, and in the opinion of the investigator would benefit from switch to a tacrolimus-based immunosuppression, will switch the immunosuppressive therapy to a tacrolimus-based one. Efficacy and safety of patients will be observed for 52 weeks.

NCT ID: NCT02263703 Completed - Clinical trials for Inflammatory Bowel Disease

Immunogenicity of HPV Vaccine in Immunosuppressed Children

Start date: May 2007
Phase: Phase 3
Study type: Interventional

Genital HPV is the necessary cause for cervical cancer, as well as a major contributing cause of several other cancers and conditions. There are now effective vaccines against the main oncogenic HPV types, HPV16 and 18. Most research and discussion has focused on targeting the vaccine to young women and older adolescents. Based on this, a national free HPV vaccination program for adolescent girls commenced in 2007, in Australia. However, at the time of commencement, there had been no research on the use of this vaccine in immunosuppressed. Therefore, information on the immunogenicity, safety and duration of efficacy of HPV vaccine when administered to immunosuppressed children is needed. This trial looked at a 3 dose schedule of quadrivalent HPV vaccine in a range of immunosuppressed children, with the endpoint being immunogenicity, followed for 5 years for duration of immunity.

NCT ID: NCT02235571 Completed - Clinical trials for Kidney Transplantation

iChoose Decision Kidney Aid for End-Stage Renal Disease Patients

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

The investigators developed iChoose Kidney -- a shared decision-making support tool accessible through iPad, iPhone, or the web -- to provide ESRD patients and their providers with a simple, standardized, easily accessible, statistically robust tool for use in the clinic to guide patient education and healthcare decision-making about treatment options of dialysis or kidney transplantation. The iChoose Kidney decision aid provides patients with estimates of their individualized 1 and 3-year risks of mortality on dialysis vs. transplantation, based on previous national data. The tool has the potential to improve communication and decision-making between patients and their healthcare providers and improve access to kidney transplantation among patients with ESRD. This will be a two-arm, randomized study, and will be conducted at 3 large transplant centers with diverse patient populations. One group of patients will receive standard education alone during their scheduled transplant evaluation. The second group will receive the standard education as well have the provider use the iChoose Kidney aid with them. The project timeline will be a total of 24 months inclusive of enrollment, follow-up, data analysis, and outcome evaluation. This study will assess how well the iChoose decision aid works in improving patient knowledge, preferences for treatment, and patient access to transplant. The study will also assess whether providers find the tool useful for providing ways to share information with patients about ways to treat their kidney disease.

NCT ID: NCT02234349 Completed - Clinical trials for Kidney Transplantation

Bile Acids and Incretins in Pancreas Kidney Transplant Patients

ITABI
Start date: September 5, 2013
Phase: N/A
Study type: Interventional

Pancreas Kidney Transplantation (PKT) is the prominent treatment for type 1 diabetic patients with chronic kidney disease and improves patients' outcome. However, in spite of an optimized systemic insulin substitution, altered glucose metabolism and beta cell function are reported in these patients. The mechanisms behind these abnormalities are still unclear. Duodena-pancreatic anastomosis is performed in a heterotopic site (ileum) and thus could change physical and chemical properties of intestinal secretions, gut flora, as well as intestinal permeability. The effect of this procedure on gut derived metabolic factors, the enterohepatic cycle of bile acids, incretin secretion and intestinal flora have never been studied. This pilot prospective, study is aimed to evaluate the modification of bile acids concentrations and composition in PKT subjects, and the impact in glucose and incretin metabolism (measured by oral glucose tolerance test) one year after transplantation. The results will be compared to those of kidney transplant patients and control subjects.

NCT ID: NCT02224144 Completed - Clinical trials for End Stage Renal Disease

Bone Mass and Strength After Kidney Transplantation

Start date: August 18, 2014
Phase: Phase 2
Study type: Interventional

The purpose of this study is to test whether active vitamin D (calcitriol) protects bones from weakening and protects blood vessels from calcium deposits over the first year of kidney transplantation.

NCT ID: NCT02217410 Completed - Clinical trials for Kidney Transplantation

CCFZ533X2201 - PoC Study in de Novo Renal Transplantation

Start date: February 5, 2015
Phase: Phase 1/Phase 2
Study type: Interventional

The purpose of this study was to investigate the safety, tolerability, pharmacokinetics (PK) and potential for CFZ533 to replace calcineurin inhibitors (CNI), while providing a similar rate of acute rejection prophylaxis and renal function in a de novo renal transplant population receiving an allograft from standard criteria donors.

NCT ID: NCT02208791 Recruiting - Clinical trials for Kidney Transplantation

Effects of the Quadruple Immunosuppression on Peripheral Blood Lymphocytes and Development of Anti-HLA Antibodies in Kidney Transplant

Start date: July 2014
Phase: Phase 4
Study type: Interventional

The purpose of this study is to determine the effects of sirolimus in the phenotype of peripheral blood T and B lymphocytes regarding their naïve, memory, effector end regulatory phenotype and in the development of anti-HLA antibodies among kidney transplant recipients with high immunological risk for graft rejection.

NCT ID: NCT02182986 Completed - Kidney Transplant Clinical Trials

Biomarkers for Post-Transplant Lymphoproliferative Disorders in Children

Start date: August 14, 2014
Phase:
Study type: Observational

Solid organ transplantation is an important therapeutic option for children with a variety of end stage diseases. However, the same immunosuppressive medications that are required to prevent the child's immune system from attacking and rejecting the transplanted organ can predispose these individuals to developing a very serious cancer that is linked to Epstein-Barr virus (EBV).

NCT ID: NCT02179411 Completed - Clinical trials for Kidney Transplant Recipients

Study of the Renal Perfusion in Healthy Volunteers and Renal Transplant Recipients During an Orthostatic Stress

ortho_rein
Start date: April 2009
Phase: N/A
Study type: Interventional

Autonomic nervous system contributes to the regulation of renal blood flow, affected by upright posture. Kidney transplantation implies sympathetic denervation. The aim of this study is to compare the renal vascular response in volunteers and renal graft recipients to an orthostatic stress induced by a head-up tilt test. Renal peripheral resistances are assessed by echo Doppler. The sympathetic nervous system activity is evaluated by plasma concentrations of catecholamine before and after the head-up tilt test.