Liver Cirrhosis Clinical Trial
Official title:
Hepatic Glucose Metabolism Measured by FDG PET/CT in Patients With Liver Disease and Healthy Subjects
The investigators wish to determine the lumped constant (LC), which is a correction factor
necessary for converting measurements of hepatic FDG metabolism (measured by PET) to those
of regular glucose in patients with cirrhosis and healthy subjects.
Working hypothesis
- LC for FDG in liver tissue is not significantly different from unity in healthy
subjects
- LC for FDG in liver disease is significantly different from LC in healthy liver
- Insulin changes the LC for FDG in liver tissue, but not by the same factor in liver
disease and healthy subjects.
The LC for FDG is determined in 8 patients with liver disease and 8 healthy volunteers with
and without glucose-clamp on two different days at 3-5 week intervals. The individual order
of the two examinations will be randomized. The subjects fast overnight before the
examination but are allowed to drink water and take usual medication.
When arriving at the PET centre, venflons are placed in a cubital vein in both arms and an
ICG infusion is started in one of them. On the day with the glucose-clamp, an infusion of
insulin and glucose is started in the second venflon. Next, an artflon is placed in one
radial artery and a lever vein catheteter is placed via an introducer catheter in the left
femoral vein under sterile conditions and local anesthetic (Lidocaine). The position of the
liver vein catheter is checked with fluoroscopy.
On each experimental day, a bolus of 200 MBq FDG + 25 μCi [3H] glucose (diluted with saline
up to 10 ml) is given intravenously at the start of a 60-min PET scan of the liver. Blood
samples from a peripheral artery and a liver vein are collected for determination of blood
concentrations of FDG and [3H]glucose at appropriate intervals.
In the experiment with glucose-clamp, an intravenous infusion of insulin (0.6 mU/kg/min) is
given and blood glucose is measured every 10 min and kept constant at around 5 mM by
infusing 20% glucose (infusion rate adjusted according to blood glucose).
During each study, the hepatic blood flow rate is measured by giving an intravenous infusion
of indocyanine green (ICG) and collecting arterial and liver vein blood samples (Fick's
principle).
Blood samples are analyzed for concentrations of FDG (gammacounter), [3H]glucose
(liquid-scintillation counter), glucose (enzymatic assay) and ICG (spectrophotometric).
When the experiment is finished, all infusions are terminated and the liver vein catheter is
removed and hemostasis ensured by manual compression (10 minutes) and bed rest for 30
minutes before the subject is allowed to stand. The artflon is then removed and hemostasis
ensured by manual compression (10 minutes). Finally, the venflons are removed.
;
Observational Model: Case Control, Time Perspective: Cross-Sectional
| Status | Clinical Trial | Phase | |
|---|---|---|---|
| Recruiting |
NCT04533932 -
Endosonographic Shear Wave Elastography for Liver Stiffness
|
||
| Not yet recruiting |
NCT06031740 -
A Comparison of Flexible Endoscopic Polidocanol Liquid and Foam Sclerotherapy in Cirrhotic Patients With Bleeding From Internal Hemorrhoids
|
N/A | |
| Not yet recruiting |
NCT06026267 -
Efficacy of Conventional Dose Protocol vs Low Dose Protocol Albumin Use in Patients With Cirrhosis and High Risk Spontaneous Bacterial Peritonitis
|
N/A | |
| Not yet recruiting |
NCT06076330 -
Efficacy of 5% Albumin v/s Plasmalyte in Combination With 20% Albumin for Fluid Resuscitation in Cirrhosis With Sepsis Induced Hypotension
|
N/A | |
| Enrolling by invitation |
NCT05055713 -
A Randomized Controlled Study on the Treatment of Cirrhosis Combined With Hypersplenism
|
N/A | |
| Recruiting |
NCT04578301 -
Predicting Acute-on-Chronic Liver Failure After Surgical Intervention in Chronic Liver Disease
|
||
| Not yet recruiting |
NCT05515861 -
Evaluation of EUS in Preventing Rebleeding After Endoscopic Cyanoacrylate Injection for Gastric Varices
|
N/A | |
| Not yet recruiting |
NCT05120557 -
Point-of-care Ultrasound Screening and Assessment of Chronic Liver Diseases and NASH
|
N/A | |
| Not yet recruiting |
NCT03623360 -
Functional MRI to Determine Severity of Cirrhosis
|
||
| Not yet recruiting |
NCT02710227 -
Sleep Timing and Circadian Preferences in A Sample of Egyptian Patients With Hepatic Cirrhosis
|
N/A | |
| Completed |
NCT02917408 -
Retrospective Study About Primary Biliary Cholangitis During January 2001 to July 2016 at West China Hospital
|
||
| Active, not recruiting |
NCT02551250 -
Annual MRI Versus Biannual US for Surveillance of Hepatocellular Carcinoma in Liver Cirrhosis
|
||
| Recruiting |
NCT02239991 -
Management of Perioperative Coagulopathy With Thromboelastometry (ROTEM) in Liver Transplant
|
N/A | |
| Enrolling by invitation |
NCT02256514 -
Open Label Trial of Immunotherapy for Advanced Liver Cancer
|
Phase 2 | |
| Terminated |
NCT02311985 -
Comparison of Three Transfusion Strategies for Central Venous Catheterization in Cirrhotics: A Randomized Clinical Trial
|
N/A | |
| Terminated |
NCT01937130 -
Pharmacokinetic and Pharmacodynamic Study of IDN-6556 in ACLF
|
Phase 2 | |
| Recruiting |
NCT01724697 -
Safety and Efficacy of Human Bone Marrow Stem Cells for Treatment of HBV-related Liver Cirrhosis
|
Phase 1/Phase 2 | |
| Recruiting |
NCT01618890 -
Hepatic Venous Pressure Gradient-guided Versus Standard Beta-blocker Therapy in Primary Prevention of Variceal Bleeding
|
Phase 3 | |
| Recruiting |
NCT01728727 -
Safety and Efficacy of Human Umbilical Cord Derived Mesenchymal Stem Cells for Treatment of HBV-related Liver Cirrhosis
|
Phase 1/Phase 2 | |
| Recruiting |
NCT01728688 -
Safety and Efficacy of Human Autologous Peripheral Blood Stem Cells for Treatment of HBV-related Liver Cirrhosis
|
Phase 1/Phase 2 |