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Liver Diseases clinical trials

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NCT ID: NCT00526331 Completed - Prostate Cancer Clinical Trials

Evaluation of Arterial Pressure Based Cardiac Output for Goal-Directed Perioperative Therapy

Start date: August 2007
Phase: Phase 4
Study type: Interventional

The purpose of this study is to determine whether the early identification and more precise intervention of operating room (OR) patient fluid administration optimization using arterial pressure-based cardiac output (APCO) yields comparable patient outcome as fluid administration optimization using a global standard care method.

NCT ID: NCT00523562 Completed - Liver Diseases Clinical Trials

Effects of Macronutrients on Hepatic Lipids, Plasma Triglycerides, and Insulin Sensitivity

MACRONUTR
Start date: July 2006
Phase: N/A
Study type: Interventional

The purpose of this study is to assess how the macronutrient composition of the diet effects - lipid and glucose metabolism - intrahepatic lipids - insulin sensitivity in healthy lean subjects and in subjects with a high metabolic risk (ie overweight and offsprings of patients with type 2 diabetes mellitus).

NCT ID: NCT00492739 Recruiting - Immunosuppression Clinical Trials

Immunity Against Varicella in Pediatric Orthotopic Liver Transplantation Recipients

VZVinOLTx
Start date: June 2007
Phase: Phase 2/Phase 3
Study type: Interventional

Varicella is a vaccine-preventable disease, which can be severe in immunosuppressed children. Currently, the (live) vaccine is not recommended in pediatric orthotopic liver transplant recipients. Furthermore, protection due to naturally acquired immunity to VZV or post-immunization isn't well described in this population.The questions asked are: - What is the influence of the immunosuppression required after orthotopic liver transplantation (OLT) on the maintenance of VZV-specific immunity elicited by wild-type varicella infection before OLT transplantation? - What is the influence of the immunosuppression required after OLT on VZV-specific immunity elicited by varicella immunization before OLT transplantation? - What is the influence of the residual immunosuppression at ≥ 12 months after OLT transplantation on the induction of VZV-specific B and T cell responses elicited by VZV vaccination after OLT transplantation? - What is the influence of the residual immunosuppression at ≥ 12 months after OLT transplantation on the persistence / waning of B and T cell responses elicited by VZV vaccination?

NCT ID: NCT00488917 Completed - Sepsis Clinical Trials

Sepsis, Endothelial Function, and Lipids in Critically Ill Patients With Liver Failure (the SELLIFA Study)

SELLIFA
Start date: June 2007
Phase: N/A
Study type: Observational

The purpose of the study is to determine the role of new biomarkers in the diagnosis of sepsis in critically-ill patients with liver failure and to correlate the prognosis of these patients with parameters of endothelial function and lipid metabolism.

NCT ID: NCT00450398 Active, not recruiting - Liver Diseases Clinical Trials

YSPSL for Prevention of Delayed Graft Function in Cadaveric Liver Transplantation

Start date: March 2007
Phase: Phase 2
Study type: Interventional

The study is designed to assess the feasibility of evaluating YSPSL for the amelioration of ischemia reperfusion injury following liver transplantation by administering YSPSL into the liver graft directly ex vivo via the portal vein and to the recipient intravenously prior to reperfusion. Recently, P-selectin expression has been associated in liver grafts with prolonged cold storage times and rejection. By examining biomarkers of IRI including P-selectin by immunohistochemistry and/or quantitative PCR, liver histology and hepatic blood flow using established techniques, the goal of this study is to evaluate the feasibility of using these modalities for future studies of safety and efficacy.

NCT ID: NCT00436722 Terminated - Liver Diseases Clinical Trials

Induction Treatment Followed by Immunosuppression Withdrawal in Liver Transplantation: A Comparative Trial

ATEGE-LIVER
Start date: June 2006
Phase: Phase 2
Study type: Interventional

This is a randomized, controlled trial in liver transplantation in which conventional immunosuppressive treatment will be compared with a therapeutic strategy consisting in pre-transplant antibody-mediated T cell depletion followed by reduced calcineurin inhibitor usage. The working hypothesis is that antibody induction followed by calcineurin inhibitor minimization may promote development of tolerogenic mechanisms allowing the eventual withdrawal of all immunosuppressive therapy.

NCT ID: NCT00426153 Completed - Liver Diseases Clinical Trials

Octreotide in Severe Polycystic Liver Disease

Start date: January 2007
Phase: Phase 2/Phase 3
Study type: Interventional

This study will evaluate the effect of Octreotide LAR® on the liver volumes of patients with severe polycystic liver disease who are not candidates or decline surgical treatments such as liver cyst fenestration, liver resection or liver transplantation. A total of 42 patients will be recruited -14 who will receive placebo and 28 the study drug. Preliminary evidence indicates that this drug is safe and non-toxic in other disease states. Treatment with this drug holds promise not only for individuals with liver involvement, but also for many more patients with polycystic kidney disease.

NCT ID: NCT00382668 Completed - Liver Diseases Clinical Trials

A Study of Dasatinib to See How Liver Impaired and Healthy Subjects Process and React to the Study Drug

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

The primary purpose of this study is to evaluate how a person with liver impairment processes and reacts to the study drug. Information about any side effects that may occur will also be collected.

NCT ID: NCT00365248 Completed - Liver Diseases Clinical Trials

TachoSil Paediatric Liver Trial (TC-019-IN)

Start date: October 2005
Phase: Phase 3
Study type: Interventional

The overall objective is to assess the haemostatic efficacy and safety of TachoSil for control of local bleeding in paediatric patients undergoing surgical resection of the liver with our without segmental liver transplantation.

NCT ID: NCT00345930 Recruiting - Liver Diseases Clinical Trials

DILIN - Prospective Study

Start date: September 2004
Phase:
Study type: Observational

The purpose of this study is to identify individuals who have suffered a liver injury arising as an idiosyncratic reaction to a prescription drug or a complementary and alternative medicine. Recently added acute cases enrollment that meets criteria to the protocol. Also added Fibroscans to the protocol that will be completed at baseline and follow-up on chronic subjects.