Patients with HCV genotype 1 and IL28B CC Polymorphism who have a rapid virological response to treatment are randomised to either 24 or 48 weeks HCV treatment. Our hypothesis is that there is no important difference in effect between the two treatment effect.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
200
patients receive a dose of 180 µg of PEGASYS once a week for 24 weeks
patients receive a dose 800 to 1200 mg of ribavirin once a day(according to weight) for 24 weeks
patients receive a dose of 180 µg of PEGASYS once a week for 48 weeks
The Eighth People's Hospital of Guangzhou
Guangzhou, Guangdong, China
RECRUITINGThe Third Affliated Hospital of Sun Yat-sen University
Guangzhou, Guangdong, China
RECRUITINGPanyu People's Hospital
Guangzhou, Guangdong, China
RECRUITINGSustained virological response (SVR)
Undetectable HCVRNA in serum(\<15IU/ml) 24 weeks after the end of treatment
Time frame: 24 weeks after the end of treatment
Change in health related quality as measured by short from 36 (SF-36) from baseline to 24 weeks after the end of treatment
Time frame: baseline, 24 weeks after the end of treatment
Sick leave in patients treated for 24 or 48 weeks treatment
Time frame: 48 weeks
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patients receive a dose 800 to 1200 mg of ribavirin once a day(according to weight) for 48 weeks
Zhongshan second people's hospital
Zhongshan, Guangdong, China
RECRUITING