Treatment Insulin Resistence in HCV G-1 Patient
Launched by VALME UNIVERSITY HOSPITAL · Oct 17, 2007
Trial Information
Current as of June 09, 2025
Completed
Keywords
ClinConnect Summary
Differents studies show that infection by virus hepatitis C have a relevant rol in the development of insulin resistance. The insulin resistence is associated with a progression of fibrosis and the development of steatosis. The insulin resistence is frecuently associated with very difficult to cure patients as cirrhotics, afro-american patients, overweight patients and co-infected HCV-HIV patients. Recently is repported that sustained virological (SVR) response in genotype 1 patients is different according the insulin resistance. The SVR was 60% in patients without insulin resistance versus...
Gender
ALL
Eligibility criteria
- Inclusion Criteria:
- • Male and female patients with 18 years of age or more
- • Serum HCV-RNA quantifiable
- • Genotype 1
- • Liver disease compensated
- • HOMA-IR \> 2
- • Treatment with Peginterferon alfa-2a + Ribavirin.
- • Negative urine or blood pregnancy test (for women of childbearing potential)
- • All fertile males and females must be using effective contraception
- Exclusion Criteria:
- • Liver chirrosis
- • Diabetes
- • Women with ongoing pregnancy or breast feeding
- • HIV positive
- • Patients who during 6 months previous to treatment loss more of 10% of weight
- • Therapy with anti-neoplasic or immunomodulatory treatment (including supraphysiologic doses of steroids and radiation) 6 months prior to the first dose of study drug
- • Any investigational drug 6 weeks prior to the first dose of study drug
- • History or other evidence of a medical condition associated with chronic liver disease other than HCV
- • Carcinoma hepatocellular
- • History or other evidence of bleeding from esophageal varices or other conditions consistent with decompensated liver disease
- • Neutrophil count \<1500 cells/mm3 or platelet count \<90,000 cells/mm3 at screening
- • Hgb \<12 g/dL in women or \<13 g/dL in men or any patient for whom anemia would be medically problematic
- • History of significant cardiac disease that could be worsened by acute anemia
- • Serum creatinine level \>1.5 times the upper limit of normal at screening
- • History of severe psychiatric disease, especially depression. Severe psychiatric disease is defined as treatment with an antidepressant medication or a major tranquilizer at therapeutic doses for major depression or psychosis, respectively, for at least 3 months at any previous time or any history of the following: a suicidal attempt, hospitalization for psychiatric disease, or a period of disability due to a psychiatric disease
- • History of a severe seizure disorder or current anticonvulsant use
- • History of immunologically mediated disease, chronic pulmonary disease associated with functional limitation, severe cardiac disease, major organ transplantation or other evidence of severe illness, malignancy, or any other conditions which would make the patient, in the opinion of the investigator, unsuitable for the study
- • History of thyroid disease poorly controlled on prescribed medications, elevated thyroid stimulating hormone (TSH) concentrations with elevation of antibodies to thyroid peroxidase and any clinical manifestations of thyroid disease
- • Evidence of severe retinopathy (e.g. CMV retinitis, macula degeneration)
- • Evidence of drug abuse (including excessive alcohol consumption) within one year of study entry
- • Inability or unwillingness to provide informed consent or abide by the requirements of the study
About Valme University Hospital
Valme University Hospital is a leading healthcare institution dedicated to advancing medical research and improving patient outcomes through rigorous clinical trials. As a prominent sponsor of innovative studies, the hospital leverages its multidisciplinary expertise and state-of-the-art facilities to facilitate groundbreaking research across various therapeutic areas. Committed to ethical standards and patient safety, Valme University Hospital collaborates with academic and industry partners to foster scientific discovery and translate findings into effective clinical practices, ultimately enhancing the quality of care provided to the community.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Barcelona, , Spain
Madrid, , Spain
Madrid, , Spain
Leon, , Spain
Madrid, , Spain
Madrid, , Spain
Madrid, , Spain
Sevilla, , Spain
Alcorcón, Madrid, Spain
Ciudad Real, , Spain
Córdoba, , Spain
Sevilla, , Spain
Málaga, , Spain
Sabadell, Barcelona, Spain
Badalona, Badalona/Barcelona, Spain
San Sebastian, , Spain
Granada, , Spain
Granada, , Spain
Valencia, , Spain
Patients applied
Trial Officials
Manuel Romero-Gomez, Dr
Study Director
Hospital Universitario de Valme. Sevilla
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported
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