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Retrospective Study to Evaluate the Impact of Using Interferon (Pegylated or Not) in the Treatment of Patients With Chronic Hepatitis C in Brazil (DECISION)
This retrospective study will assess the sustained virologic response and the safety of two different interferons (pegylated or conventional) in patients with chronic hepatitis C. Data will be collected for 24 weeks.
Age
18 - 70 years
Sex
ALL
Healthy Volunteers
No
Rio Branco, Acre, Brazil
Manaus, Amazonas, Brazil
Vitória, Espírito Santo, Brazil
Salvador, Estado de Bahia, Brazil
Goiânia, Goiás, Brazil
São Luís, Maranhão, Brazil
Campo Grande - MS, Mato Grosso do Sul, Brazil
Pouso Alegre, Minas Gerais, Brazil
Uberaba, Minas Gerais, Brazil
Curitiba, Paraná, Brazil
Start Date
January 1, 2010
Primary Completion Date
November 1, 2012
Completion Date
June 1, 2013
Last Updated
November 29, 2016
660
ACTUAL participants
Conventional Interferon
DRUG
Peginterferon Alfa-2a
DRUG
Peginterferon Alfa-2b
DRUG
Ribavirin
DRUG
Lead Sponsor
Hoffmann-La Roche
NCT05870969
NCT03987503
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.
View ClinicalTrials.gov Terms and ConditionsNCT04382404