Timing and Duration of Acute Hepatitis C Treatment
Phase IV Study of Treatment of Acute Hepatitis C With Pegylated Interferon
6 other identifiers
interventional
180
1 country
3
Brief Summary
Spontaneous resolution of acute hepatitis C infection cannot be predicted and the majority of cases persist and become chronic. This randomized trial assesses the efficacy and safety of peginterferon alfa-2b. The investigators hypothesize that therapy strategies could prevent the development of chronic hepatitis.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for phase_4
Started Jan 2002
Longer than P75 for phase_4
3 active sites
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
Study Start
First participant enrolled
January 1, 2002
CompletedFirst Submitted
Initial submission to the registry
October 18, 2005
CompletedFirst Posted
Study publicly available on registry
October 19, 2005
CompletedStudy Completion
Last participant's last visit for all outcomes
January 1, 2006
CompletedSeptember 11, 2006
September 1, 2006
October 18, 2005
September 7, 2006
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Sustained viral response rate in treatment group versus control
Secondary Outcomes (3)
End of treatment virologic response
Early virologic response at week 4
Quality of life
Interventions
Eligibility Criteria
You may qualify if:
- Age: 18-50 years, with or without symptoms
- Diagnosis of acute hepatitis C: elevated serum alanine aminotransferase (ALT) \> 10 times the upper limit of normal (ULN)
- Seroconversion from negative to positive anti-HCV antibody status (third-generation enzyme-linked immunosorbent assay)
- Conversion from negative to positive polymerase chain reaction (PCR) for HCV-RNA, ruling out other causes of hepatitis by history and appropriate serologic and virologic studies.
You may not qualify if:
- Decompensated liver disease
- Coinfection with human immunodeficiency virus (HIV) or Schistosoma mansoni
- Marked anemia (hemoglobin level ≤ 120 g/L in women and ≤ 130 g/L in men)
- Neutropenia (\< 1,500/mm3)
- Thrombocytopenia (\< 90,000/mm3)
- A creatinine concentration \> 1.5 times ULN
- Serum alpha-fetoprotein \> 25 ng/ml
- An organ transplant
- Neoplastic disease
- Severe cardiac or pulmonary disease
- Unstable thyroid dysfunction
- A psychiatric disorder
- Seizure disorder
- Severe retinopathy
- A current pregnancy or were breast feeding or unwillingness to practice contraception
- +2 more criteria
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Ain Shams Universitylead
- University Hospital Freiburgcollaborator
- Beth Israel Deaconess Medical Centercollaborator
- Alexander von Humboldt Associationcollaborator
- Fulbrightcollaborator
- National Institute of Allergy and Infectious Diseases (NIAID)collaborator
- Tempus AIcollaborator
- International Society for Infectious Diseasescollaborator
Study Sites (3)
ASU Specialized Hospital
Cairo, Cairo Governorate, 11351, Egypt
ASU
Cairo, 03316, Egypt
Shebin Liver Center
Cairo, 11351, Egypt
Related Publications (9)
Kamal SM, Ismail A, Graham CS, He Q, Rasenack JW, Peters T, Tawil AA, Fehr JJ, Khalifa Kel S, Madwar MM, Koziel MJ. Pegylated interferon alpha therapy in acute hepatitis C: relation to hepatitis C virus-specific T cell response kinetics. Hepatology. 2004 Jun;39(6):1721-31. doi: 10.1002/hep.20266.
PMID: 15185314BACKGROUNDGerlach JT, Diepolder HM, Zachoval R, Gruener NH, Jung MC, Ulsenheimer A, Schraut WW, Schirren CA, Waechtler M, Backmund M, Pape GR. Acute hepatitis C: high rate of both spontaneous and treatment-induced viral clearance. Gastroenterology. 2003 Jul;125(1):80-8. doi: 10.1016/s0016-5085(03)00668-1.
PMID: 12851873BACKGROUNDNomura H, Sou S, Tanimoto H, Nagahama T, Kimura Y, Hayashi J, Ishibashi H, Kashiwagi S. Short-term interferon-alfa therapy for acute hepatitis C: a randomized controlled trial. Hepatology. 2004 May;39(5):1213-9. doi: 10.1002/hep.20196.
PMID: 15122749BACKGROUNDKamal SM, Rasenack JW, Bianchi L, Al Tawil A, El Sayed Khalifa K, Peter T, Mansour H, Ezzat W, Koziel M. Acute hepatitis C without and with schistosomiasis: correlation with hepatitis C-specific CD4(+) T-cell and cytokine response. Gastroenterology. 2001 Sep;121(3):646-56. doi: 10.1053/gast.2001.27024.
PMID: 11522749BACKGROUNDSantantonio T, Sinisi E, Guastadisegni A, Casalino C, Mazzola M, Gentile A, Leandro G, Pastore G. Natural course of acute hepatitis C: a long-term prospective study. Dig Liver Dis. 2003 Feb;35(2):104-13. doi: 10.1016/s1590-8658(03)00007-0.
PMID: 12747629BACKGROUNDWiegand J, Jackel E, Cornberg M, Hinrichsen H, Dietrich M, Kroeger J, Fritsch WP, Kubitschke A, Aslan N, Tillmann HL, Manns MP, Wedemeyer H. Long-term follow-up after successful interferon therapy of acute hepatitis C. Hepatology. 2004 Jul;40(1):98-107. doi: 10.1002/hep.20291.
PMID: 15239091BACKGROUNDKamal SM, El Tawil AA, Nakano T, He Q, Rasenack J, Hakam SA, Saleh WA, Ismail A, Aziz AA, Madwar MA. Peginterferon alpha-2b and ribavirin therapy in chronic hepatitis C genotype 4: impact of treatment duration and viral kinetics on sustained virological response. Gut. 2005 Jun;54(6):858-66. doi: 10.1136/gut.2004.057182.
PMID: 15888797BACKGROUNDJaeckel E, Cornberg M, Wedemeyer H, Santantonio T, Mayer J, Zankel M, Pastore G, Dietrich M, Trautwein C, Manns MP; German Acute Hepatitis C Therapy Group. Treatment of acute hepatitis C with interferon alfa-2b. N Engl J Med. 2001 Nov 15;345(20):1452-7. doi: 10.1056/NEJMoa011232.
PMID: 11794193BACKGROUNDLarghi A, Zuin M, Crosignani A, Ribero ML, Pipia C, Battezzati PM, Binelli G, Donato F, Zanetti AR, Podda M, Tagger A. Outcome of an outbreak of acute hepatitis C among healthy volunteers participating in pharmacokinetics studies. Hepatology. 2002 Oct;36(4 Pt 1):993-1000. doi: 10.1053/jhep.2002.36129.
PMID: 12297849BACKGROUND
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Study Officials
- STUDY CHAIR
Alaa Ismail, M.D.
Ain Shams University
- PRINCIPAL INVESTIGATOR
Sanaa M Kamal, M.D.
Ain Shams University
- PRINCIPAL INVESTIGATOR
Nezam H Afdhal, M.D.
Harvard Medical School (HMS and HSDM)
- PRINCIPAL INVESTIGATOR
Manal El Sayed, M.D.
ASU
Study Design
- Study Type
- interventional
- Phase
- phase 4
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
Study Record Dates
First Submitted
October 18, 2005
First Posted
October 19, 2005
Study Start
January 1, 2002
Study Completion
January 1, 2006
Last Updated
September 11, 2006
Record last verified: 2006-09