Liver Disease Related Trials
For more information regarding these clinical trials,
please call 303-315-1135.
| Name | Principal Investigator |
|---|---|
Utility of transarterial chemoembolization for hepatocellular carcinoma in the liver transplant candidate: an intention- to- transplant analysis |
|
Accuracy of pre-transplantation diagnosis of hepatocellular carcinoma based on imaging and clinical presentation: comparison with explant histology |
|
Increased immunosuppressant levels in hepatitis C liver transplant recipients |
|
Treatment of hepatitis C virus (HCV) following liver transplantation |
|
Adult to adult living donor liver transplantation (A2ALL) cohort study: retrospective study protocol (A2ALL RETRO-01) |
|
Transjugular intrahepatic portosystemic shunt (TIPS) versus liver transplantation in the treatment of Budd-Chiari syndrome: experience at our institution and a review of the literature |
Augustin R. Attwell, MD |
Significant disparity in MELD (Model for Endstage Liver Disease) scores of liver transplantation recipients based on size of waiting list: impact of organ allocation and patient outcomes |
|
Characteristics of liver transplantation centers performing adult to adult living donor transplantation |
|
Gallbladder stent placement for the treatment of symptomatic gallstone disease in patients with cirrhosis |
|
A patient survey of metabolic complications after liver transplantation: determination of perceptions regarding complications and their management practice patterns |
|
Metabolic complications after liver transplantation: characterization and determination of physician attitudes and practice patterns |
|
Pre-study serial histology as a predictor of response to continuous therapy during the HALT-C trial |
|
Quantitative assessment of hepatic function in chronic HCV |
|
A randomized, double blind trial of telbivudine (LDT) versus Lamivudine in adults with decompensated chronic hepatitis B and evidence of cirrhosis |
|
A double blind, randomized, placebo-controlled, multi-centre, dose ranging, parallel group, Phase II study to assess efficacy, safety/tolerability, and pharmacokinetics of a thrombopoietin receptor agonist, SB-497115-GR, when administered as 30, 50, 75 MG once daily for 12 weeks in subjects with chronic hepatitis C-related thrombocytopenia who are potential candidates for antiviral treatment with pegylated interferon and ribavirin |
|
The A2ALL LADR protocol: pre-transplant treatment to prevent recurrence of hepatitis C after living donor liver transplantation |
|
Liver recipients in the HCUP database: a study of hospital utilization and costs |
|
A prospective, randomized, multicenter, open-label, comparative safety and efficacy study of prophylactically administered pegylated interferon Alfa-2A (Pegasys) plus ribavirin vs. no prophylaxis following liver transplantation for hepatitis C. |
|
The pharmacokinetics of myfortic (mycophenolic acid) in liver transplant recipients |
|
The hepatitis C antiviral long-term treatment to prevent cirrhosis (Halt-C) trial: a randomized controlled trial to evaluate the safety and efficacy of long-term peginterferon Alfa-2A for treatment of chronic hepatitis C in patients who failed to respond to previous interferon therapy |
|
Adult to adult living donor liver transplant cohort study |
|
A Phase I double blind, placebo controlled, dose escalation, multicenter therapeutic trial of the safety, immunogenicity, and efficacy of GI-5005; an inactivated recombinant saccharomyces cerevisiae expressing a hepatitis C virus NS3-core fusion protein, in patients with chronic hepatitis C infection |
|
Immune responses in acute hepatitis C infection |
|
A Phase II trial to assess the safety of immunosuppression withdrawal in liver transplant recipients with hepatitis C |
|
A prospective, open-label, multi center, randomized trial of the efficacy and safety of a long term calcineurin inhibitor free maintenance regime with mycophenolate mofetil and sirolimus in recipients of an orthotopic liver transplant |
|
Hepatic research registry |
|
A double blind, placebo controlled, randomized Phase III study of intravenous terlipressin in patients with hepatorenal syndrome type I. |
|
A pilot study for the use of the secure continuous remote alcohol monitor (SCRAM) in patients listed for liver transplantation |
|
HCV RNA testing in Halt-C sustained virologic responders |
|
PVCLD national registry database for pulmonary vascular complications of liver disease |
|
Restoration of hepatic function in living liver donors (an ancillary study of A2ALL) |
|
A phase II multicenter trial to assess the safety and efficacy of campth-1H and tacrolimus followed by immunosuppression withdrawal in liver transplantation |
|
Hepatitis C immunity in the human liver transplant model |
|
Randomized evaluation of fibrosis due to hepatitis C after de novo liver transplant (refine) a multicenter, randomized, open-label study to compare the development of liver fibrosis at 12 months after transplantation for hepatitis C cirrhosis in patients receiving either neural or tracrolimus |
|
Protocol for the collection of specimens used in Abbott laboratories in vitro diagnostic hepatitis assay clinical studies (7B5-02-04Z01-01) |
|
A randomized, controlled, multicenter study of thymoglobulin induction therapy with a calcineurin-inhibitor sparing regimen in liver transplant patients |
|
Changes of metabolic profiles in urine from long-term liver transplant patients as a potential marker for immunosuppressant nephrotoxicity |
|
Changes of metabolic profiles in urine from de novo liver transplant patients during the first 12 months after transplantation as a potential marker of immunosuppressant nephrotoxicity |
