Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
1210 participants
OBSERVATIONAL
2015-05-15
2024-07-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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COHORT
OTHER
Eligibility Criteria
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Inclusion Criteria
* Provide written, informed consent;
* Be willing and able to comply with the visit schedule and protocol-mandated procedures.
Exclusion Criteria
* History of clinically significant illness or any other major medical disorder that may interfere with follow up, assessments, or compliance with the protocol.
* Inability to provide written informed consent.
18 Years
ALL
No
Sponsors
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Beijing 302 Hospital
OTHER
Nanfang Hospital, Southern Medical University
OTHER
Yamanashi Prefectural Central Hospital
UNKNOWN
Humanity and Health Research Centre
OTHER
Responsible Party
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Principal Investigators
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George Lau, MD
Role: PRINCIPAL_INVESTIGATOR
Humanity & Health Medical Centre
Locations
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Liver Fibrosis Diagnosis and Treatment Centre, 302 Hospital
Beijing, Beijing Municipality, China
Humanity and Health GI and Liver Centre
Hong Kong, Hong Kong, China
Yamanashi Prefectural Central Hospital
Kofu, Yamanashi, Japan
Countries
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Other Identifiers
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H&H_HCV IFN Vs DAAs Fu
Identifier Type: -
Identifier Source: org_study_id
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