Chronic Hepatitis C Clinical Trial
Official title:
Investigating the Effects of Camel Milk Products on the Laboratory Markers in the Patients With Chronic Hepatitis C, Genotype 2 & 3
Camel milk as the new modality for treatment of chronic hepatitis C. The purpose of this study is to evaluate effectiveness and safety of camel milk in combination with Peginterferon Alfa-2a and Ribavirin in genotype 2,3 chronic hepatitis C virus .
The investigators enrolled 40 patients into the study. Group 1(Intervention ) : received
PEGASYS( Peginterferon ) One subcutaneous injection containing 0.5 ml solution with180 mcg
per week plus COPEGUS( Ribavirin ) tablets (body-weight adjusted dose: < 75 kg = 1000 mg and
≥ 75 kg = 1200 mg) taken orally (by mouth) once daily and 250 ml of raw camel milk will be
consumed in 10 minutes orally twice daily for 12 weeks.
Group 2 ( control ): received PEGASYS( Peginterferon ) One subcutaneous injection containing
0.5 ml solution with180 mcg per week plus COPEGUS( Ribavirin ) tablets (body-weight adjusted
dose: < 75 kg = 1000 mg and ≥ 75 kg = 1200 mg) taken orally (by mouth) once daily for 12
weeks.
Follow up period is 1,2,3 months after treatment. The patients are visited every 4 weeks
with biochemistry lab tests. The patients are checked with quantitative HCV RNA (Ribonucleic
Acid) on the first months after initiation of the treatment to assess early virologic
response and at the end of the study for complete response rate and on the third month after
treatment completion for sustained response rate. The patients with undetectable HCV RNA are
considered as responders.
;
Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment
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