About this trial
The objectives of this study are to improve HCV linkage-to-care in Chinese women and provide theoretical basis for the scientific formulation of HCV prevention and control strategies for pregnant women.
To understand the epidemiological changes and status of hepatitis C virus (HCV) infection in pregnant women in Shaanxi province in recent 10 years, and to analyze the main influencing factors of hepatitis C infection in pregnant women.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Pregnant women or parturient women confirmed by blood HCG test.
Patients aged 18 years old and above.
Patients with HCV antibody seropositive or HCV RNA positive from 2014-2023.
Disqualifiers
Patients without valid telephone numbers.
Duplicate records: For duplicate records of the same pregnant woman, only one record should be kept.
Trial population
Pregnant women who had an antenatal visit or gave birth between 2014 and 2023.
Trial design
Cohort
Retrospective
Treatments tested in this trial
Standard Direct-acting antivirals (DAA) treatment procedures for patients with hepatitis C
Procedure/SurgeryInitiated Standard DAA treatment among HCV RNA positive patients.
Treatment groups
Trial outcomes
Primary outcomes
Relink rate
The percentage of patients receiving DAA treatment among the diagnosed but untreated patients.
Locations
Sponsors and contacts
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This trial is not recruiting at the moment. You can still explore other options: