Longitudinal cohort to evaluate Hepatitis C treatment effectiveness in HIV co-infected patients: Manipur, India

Research Protocol4. OBJECTIVES\ud Primary objective\ud The primary objective of this study is to assess the effectiveness of HCV curative treatments in\ud patients with chronic hepatitis C (CHC), co-infected with HIV in Manipur, India.\ud Secondary objectives\ud a. To describe the demographic, clinical and biological characteristics of patients with chronic\ud hepatitis C and HIV co-infection\ud b. To assess the effectiveness of HCV curative strategies in patients with chronic HCV, co-infected\ud with HIV stratified by regimen and by site\ud c. To identify risk factors associated with differing virological responses\ud d. To assess the safety of HCV treatment\ud e. To monitor the safety of HCV treatment in HIV co-infected patients\ud f. To document the clinical and biological tolerance of the HCV treatment\ud g. To assess the feasibility of HCV treatment\ud h. To assess comparative performance of elastography (Fibroscan®) and APRI (AST to Platelet\ud Ration Index), to evaluate liver fibrosis among HIV/HCV co-infected individuals\ud i. To describe causes of non-eligibility for treatment\ud j. To describe the clinical and biological evolution of co-infected patients, not eligible for HCV\ud treatment\ud k. To assess treatment adherenc