Hepatitis C is the most common reason for liver transplantation in the United States and affects nearly 4 million Americans. Treatments for hepatitis C are available but are poorly tolerated and are not always effective. Morbidity and mortality from hepatitis C are related to the development and progression of hepatic fibrosis to cirrhosis and end stage liver disease. Efforts to block progression of liver disease would thus result in prevention of morbidity and mortality as well as costs incurred by the health system in the care of these conditions. Scar tissue in the liver is secreted by a type of cell, called the stellate cell, in an activated state. This cell carries a receptor for angiotensin, a hormone, when activated. If this receptor is blocked, the cell becomes inactive and does not participate in scar tissue formation. Thus, we hypothesize that using a drug such as candesartan, which blocks angiotensin receptors, should result in less scar tissue formation in the livers of patients with hepatitis C.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
16mg po daily
once daily
Kaiser Permanente
Roseville, California, United States
Kaiser Permanente
Sacramento, California, United States
Primary: • Stellate cell activity by alpha SMA stain quantitated by morphometry
Time frame: 48 weeks
• Hepatic fibrosis by morphometry
Time frame: 48 weeks
Surrogate markers for fibrosis (liver TGF-beta levels, serum procollagen-III peptide levels)
Time frame: 48 weeks
Functional status- Albumin, INR, T. Bilirubin, MELD score
Time frame: 48 weeks
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.