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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05446532
Other study ID # 2022/5032
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date June 15, 2022
Est. completion date December 31, 2022

Study information

Verified date July 2022
Source Corporacion Parc Tauli
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

HBV infection is a dynamic process with complex interactions between virus replication and the host's immune response. The appearance of anti-HBs after HBV infection generally indicates recovery and immunity to HBV1 infection. However, there are several published studies that describe the coexistence of the marker of chronic infection (HBsAg +) and the marker of functional cure (HBsAc +). There are contradictory studies on whether the coexistence of HBsAg/HBsAc implies a different clinical course.


Recruitment information / eligibility

Status Recruiting
Enrollment 120
Est. completion date December 31, 2022
Est. primary completion date October 31, 2022
Accepts healthy volunteers No
Gender All
Age group 18 Years to 90 Years
Eligibility Inclusion Criteria: - all those patients who have been seen in outpatient hepatology consultations and who present positive HBsAg and HBsAc serology simultaneously. Exclusion Criteria: - Hepatitis C or HIV Co-infection

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
Spain H. Consorci Sanitari Parc Tauli Sabadell Barcelona

Sponsors (6)

Lead Sponsor Collaborator
Corporacion Parc Tauli Consorci Hospitalari de Vic, Consorci Sanitari de Terrassa, Germans Trias i Pujol Hospital, Hospital Mutua de Terrassa, Hospital Universitario La Fe

Country where clinical trial is conducted

Spain, 

Outcome

Type Measure Description Time frame Safety issue
Primary prevalence concomitant HBsAg and HBsAc markers To describe the prevalence of concomitant HBsAg and HBsAc markers in our area 10 years
Secondary differences between immunocompetent patients with respect to immunocompromised ones. To compare if there are differences in the prevalence or clinical outcome according if the patient has any degree of immunosupresion or not. 10 years
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