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Liver Transplantation clinical trials

View clinical trials related to Liver Transplantation.

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NCT ID: NCT04246970 Enrolling by invitation - Cirrhosis, Liver Clinical Trials

Prehabilitation and Posttransplant Training Program in Liver Transplantation

PreLiveR-T
Start date: April 1, 2021
Phase: N/A
Study type: Interventional

PreLiveR-T consists of a prospective randomized clinical trial conducted in an adult population that is a candidate for liver transplantation (LT) at the Hospital La Fe Valencia (Spain). The study is structured in three phases: I) Prehabilitation (2 months before LT); II) Training, divided in two successive periods: Supervised training (months 3-6 after LT) and Unsupervised training (6-12 months after LT); III) Long-term follow-up (2 years after LT). Primary outcomes are related to post-surgery evolution (morbidity and mortality, hospitalization length, etc.). As a secondary outcomes are collected those related to: functional capacity, muscle strength and quality of life.

NCT ID: NCT04230707 Enrolling by invitation - Anxiety Clinical Trials

Endogenous Melatonin Levels on Anxiety in Living Liver Donors

Start date: October 1, 2019
Phase:
Study type: Observational

Interesting in living liver donor transplantation have greatly increased because of inadequacy of cadaveric organs and the inability to supply the growing need for cadaveric transplantation. Surgical procedures applied to living liver donors do not only physically demand organs, but can also cause psychological burden. It has been reported that melatonin had antioxidant, antinociceptive, hypnotic, anticonvulsant, neuroprotective, anxiolytic, sedative and analgesic properties. It was shown to administration of exogenous melatonin has been increase sedation and decrease anxiety in the preoperative period compared to placebo. The aim of this study; To investigate preoperative and postoperative anxiety levels of CKV and to exam the relationship between anxiety levels and endogenous melatonin levels.

NCT ID: NCT04069065 Enrolling by invitation - Liver Transplant Clinical Trials

Efficacy and Safety of Once-Daily Tacrolimus in Liver Transplant Recipients (SOUL)

Start date: July 31, 2019
Phase: Phase 4
Study type: Interventional

The purpose of this study is to evaluate the efficacy and safety of conversion to TacroBell slow-release cap.(Once-daily Tacrolimus) in patients undergoing maintenance therapy with Twice-Daily Tacrolimus after liver transplantation.

NCT ID: NCT03024840 Enrolling by invitation - Clinical trials for Liver Transplantation

Anaesthetic and Pediatric Living Related Liver Transplantation

Start date: December 2016
Phase: N/A
Study type: Interventional

To study the effect of different anaesthetic methods on pediatric neurocognitive development and cerebral injury during pediatric living related liver transplantation .

NCT ID: NCT01117077 Enrolling by invitation - Clinical trials for Liver Transplantation

The Immune Tolerance Mechanism Induced by IL-17-producing Regulatory T Cells in the Orthotopic Liver Transplant Recipients With Aspergillosis

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

Infection accounted for the first cause of death in patients after liver transplantation, and 2 / 3 of the cause of death was fungal infections. The investigators group early found that T cell subsets playing a role of inducing immune tolerance were significantly increased in vivo of liver transplantation patients with aspergillus infection, which may be a kind of Treg cells expressing IL-17. To explore the immune tolerance mechanism induced by the immune balance cells is important to liver transplantation patients for improving efficacy and reducing the mortality. Therefore, the investigators are going to get the blood sample and liver tissue of the liver transplantation patients before and after treatment of aspergillus infection, flow cytometry analysis of blood T cell subsets, Cytometric Bead Array to detect changes in blood cytokines, laser capture microdissection to obtain liver biopsies of inflammatory cells in portal area and further for analysis of T cell subsets and protein. And the investigators are also to investigate the characteristics of CCR6 + CD4 + FOXP3 + Treg cell clones secreting IL-17 and the capacity of which suppressing conventional T cell proliferation. This study may find new methods, such as certain types of T cell subsets or cytokines for the treatment of liver transplant patients, which not only to anti-rejection but also to reduce fungal infection.

NCT ID: NCT00701272 Enrolling by invitation - Hepatitis C Clinical Trials

FGL2/Fibroleukin and Hepatitis C Virus Recurrence Post Liver Transplantation

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

The main objective of this study is to assess whether a recently-developed bioassay for the molecule "secreted fibrinogen-like protein 2" (sFGL2) can be used to predict the recurrence and/or progression of Hepatitis C Virus disease in post liver transplant patients. The hypothesis is that patients with chronic HCV have higher than normal levels of sFGL2 in their blood both pre- and post-transplantation and that this will inhibit their ability to clear HCV, and influence the progression of HCV disease when it recurs.

NCT ID: NCT00646685 Enrolling by invitation - Clinical trials for Liver Transplantation

Duct-to-duct vs Roux-en-y Hepaticojejunostomy for Biliary Reconstruction in Adult Living Donor Liver Transplantation

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

The purpose of this study is to empirically determine whether one of 2 surgical techniques commonly used for bile duct reconstruction during living donor liver transplantation results in fewer biliary complications. Also, this study may identify patient group(s) that particularly benefit from a particular technique.

NCT ID: NCT00564538 Enrolling by invitation - Clinical trials for Liver Transplantation

A Study of Thymoglobulin and Tacrolimus in Liver Transplant

thymo
Start date: December 2007
Phase: Phase 4
Study type: Interventional

The purpose of this study is to compare kidney function, long term patient and graft survival, and incidence of acute rejection in liver transplant recipients between one group receiving thymoglobulin induction and delayed initiation of tacrolimus and another group of liver transplant recipients having immediate administration of tacrolimus without any induction immunosuppression.