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Liver Transplantation clinical trials

View clinical trials related to Liver Transplantation.

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NCT ID: NCT01001403 Completed - Clinical trials for Liver Transplantation

Effect of Nafamostat on Postreperfusion Syndrome (PRS)

Start date: March 2009
Phase: Phase 4
Study type: Interventional

This study intends to see the effect of nafamostat on the attenuation of postreperfusion syndrome (PRS) that frequently occurs during liver transplantation.

NCT ID: NCT00995956 Completed - Liver Transplant Clinical Trials

Albumin, Total and Free Fraction of Mycophenolic Acid, and Measurement of IMPDH Activity in Liver Transplants.

Albumix
Start date: January 2010
Phase: N/A
Study type: Observational

In this study we aim to investigate to what extent the serum albumin concentration in liver transplant patients treated with mycophenolic acid (MPA) affect the free fraction of MPA. Furthermore we will investigate if a change in free fraction has implications for the immunosuppressive effect of MPA by measuring the IMPDH activity. This might in the future provide opportunity for further individualisation of the treatment with MPA. We will also investigate if the stabilizers present in pharmaceutical-grade albumin have a displacement effect on MPA in Vitro (ref).

NCT ID: NCT00990470 Completed - Clinical trials for Liver Transplantation

Endoscopic Evaluation in Transplantation Candidates

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

In consideration of the limited supply of donor organs, the careful selection of transplant candidates is essential to optimize patient outcome after transplantation. Therefore an extensive evaluation of transplant candidates including among others esophagogastroduodenoscopy (EGD) and colonoscopy has been implemented in our centre. The data regarding the prevalence of upper and lower gastrointestinal (GI) pathology in transplant candidates are contradictory and are based on only a few retrospective studies, which often include only a subgroup of transplant candidates. The goal of this project is a prospective evaluation of the frequency of GI pathologies in transplant candidates with specific focus on the following questions: 1. Are there GI-pathologies that occur at a higher prevalence in transplant candidates than described in the general population and is there an increase of GI-pathologies since the introduction of the urgency-based organ allocation leading to sicker transplant candidates? 2. What is the influence of endoscopic findings on patient management before transplantation? 3. Which risk factors can be identified that predict the presence of GI-lesions? 4. Is there a subgroup of patients, in which screening colonoscopy before liver transplantation can not be recommended considering the cost/benefit ratio? 5. Is there a correlation of endoscopic findings with outcome after liver transplantation or with gastrointestinal complications during or after transplantation (e.g. gastrointestinal bleeding, perforation or gastrointestinal malignancy)?

NCT ID: NCT00970073 Completed - Clinical trials for Liver Transplantation

Low Dose Thymoglobulin to Protect Kidney Function After Liver Transplant

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

This study will evaluate the use of a drug called Thymoglobulin, combined with a delayed start of the anti-rejection drugs (10 days after liver transplant), compared to the current approach of starting anti-rejection drugs called calcineurin inhibitors or CNI's within 2 days after the liver transplant.

NCT ID: NCT00938860 Completed - Hepatitis C Clinical Trials

Sustained Virological Response (SVR) to Antiviral Treatment of Liver Transplant Recipients With Recurrent Hepatitis C

SUSTAIN
Start date: September 2009
Phase: Phase 4
Study type: Interventional

This study will assess the rates of Sustained Virological Response following anti-viral therapy with Peg-Interferon plus Ribavirin in patients that have been liver transplanted with recurrent Hepatitis C and treated with Neoral or tacrolimus.

NCT ID: NCT00909571 Completed - Clinical trials for Liver Transplantation

Pharmacokinetics of Tacrolimus in Liver Transplantation Patients Treated With Prograf and Modified Release Tacrolimus

Start date: April 2009
Phase: Phase 3
Study type: Interventional

Tacrolimus pharmacokinetics study in primary living donor liver transplantation patients with Tacrolimus based immunosuppressive regimens.

NCT ID: NCT00879268 Completed - Clinical trials for Liver Transplantation

Vasosol Organ Perfusion Solution and Medtronic Portable Bypass System

Start date: July 2004
Phase: Phase 1
Study type: Interventional

This is a pilot trial of centrifugal machine preservation of donor livers for transplantation using a novel preservation solution.

NCT ID: NCT00839709 Completed - Clinical trials for Liver Transplantation

Peripheral Immunologic Response of Solid Organ Transplant Recipients to Depletion Versus Non-depletion Protocols

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

Rejection and infection are primary causes of morbidity and mortality in solid organ transplant recipients. Current clinical practice relies on immunosuppressive drug levels measured in plasma to reflect the peripheral immune response in solid organ transplant recipients. Direct measurement of the number and functions of the immune cells themselves using multi-parameter flow cytometry may enable individualized immunosuppression management for organ transplant recipients. Multi-parameter flow cytometry will be used to compare levels and functional capabilities of multiple lymphocyte subsets between cohorts of patients receiving depletion induction and those receiving a non-depletion regimen. The activation state, cytotoxic potential and the functional capabilities of these cells will be examined within patients over the first six months post transplant.

NCT ID: NCT00780026 Completed - Liver Transplant Clinical Trials

Intraoperative Glucose Control in Liver Transplant

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

The goal of the proposed study is to evaluate the effectiveness of intraoperative, strict glycemic control to improve survival and infection rates following liver transplantation in a randomized, prospective trial.Primary objective: To determine if strict intraoperative blood glucose control, when compared to standard intraoperative glycemic control, improves 1-year recipient survival and decreases surgical complications, including infections, following liver transplantation.

NCT ID: NCT00778687 Completed - Clinical trials for Liver Transplantation

Heart Rate Variability Change After Liver Transplantation

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

Cirrhotic cardiomyopathy describes a hyperdynamic state with the presentation of high cardiac output and low systemic vascular resistance. And the latent heart failure becomes obvious under physiologic and pharmacologic stress. The goal of our study is to assess the effects of liver transplantation on the heart rate variability in patients with end stage liver disease.