HBV Reactivation in Immunocompromised Patients (REANT STUDY)

ConditionHBV
Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18-80
SponsorYaşar Bayındır, MD

About this trial

Background/Objective: Comorbidities represent a critical risk factor in the prognosis of patients receiving immunosuppressive therapy. For patients with anti-HBc IgG positivity requiring Hepatitis B virus (HBV) prophylaxis, the long-term physiological impact of oral antivirals remains a concern. This study aims to prospectively monitor bone, renal, and metabolic dysfunctions associated with oral antiviral use and other systemic risk factors over a long-term period.

Methods: The REANT Cohort is designed as a 4-year, multicenter prospective study. The cohort will consist of patients initiated on HBV prophylaxis due to immunosuppressive treatment. Participants will undergo regular longitudinal assessments to evaluate bone mineral density, renal filtration and tubular functions, and metabolic profiles. The interplay between antiviral therapy, baseline comorbidities, and long-term organ dysfunction will be analyzed.

Conclusion: The findings from the REANT Cohort are expected to provide robust evidence regarding the safety of long-term HBV prophylaxis and assist in the development of monitoring guidelines for immunosuppressed patients with latent HBV infection.

Eligibility criteria

Qualifiers

Aged 18 years or older

Positive for Anti-HBc IgG

Must be candidate for immunosuppressive therapy.

Disqualifiers

Voluntary Withdrawal

Failure to attend follow-up visits

Trial design

Treatments tested in this trial

  • Antiviral

Treatment groups

No treatment groups listed

Sponsors and collaborators

Yaşar Bayındır, MD

Lead sponsor

Guven Health Group

Sponsor institution

SOUTHEAST NEUROLOGY AND INFECTIOUS DISEASES SOCIETY

Collaborator