Actively Recruiting

Age: 18Years +
All Genders
Healthy Volunteers
NCT07491848

Oral-Periodontal Evaluation and Assessment of Oral Fluid Biomarkers in Patients With Hepatitis B+D

Led by Research Center of Periodontal-Systemic Interactions · Updated on 2026-03-25

25

Participants Needed

2

Research Sites

52 weeks

Total Duration

On this page

Sponsors

R

Research Center of Periodontal-Systemic Interactions

Lead Sponsor

U

University of Medicine and Pharmacy Craiova

Collaborating Sponsor

AI-Summary

What this Trial Is About

Periodontal disease is a chronic inflammatory condition associated with systemic diseases, highlighting the concept of periodontal medicine. This study aims to investigate the relationship between periodontal inflammation, oral lesions, and hepatitis B+D infection, with or without bulevirtide treatment. Oral-periodontal clinical parameters and targeted inflammatory biomarkers in saliva and gingival crevicular fluid will be evaluated in three groups: patients with hepatitis B+D receiving bulevirtide, patients with hepatitis B+D not receiving bulevirtide, and healthy controls.

CONDITIONS

Official Title

Oral-Periodontal Evaluation and Assessment of Oral Fluid Biomarkers in Patients With Hepatitis B+D

Who Can Participate

Age: 18Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Adults (≥18 years old) capable of providing informed consent
  • Confirmed co-infection with hepatitis B and D for hepatitis B+D groups
  • Receiving bulevirtide therapy for the bulevirtide group
  • Not receiving bulevirtide for the no bulevirtide group
  • Systemically healthy adults without hepatitis B or D infection for the healthy control group
  • Willingness to undergo oral-periodontal exams, saliva and gingival fluid collection, and oral photography
Not Eligible

You will not qualify if you...

  • Presence of other systemic diseases affecting periodontal health (e.g., uncontrolled diabetes, autoimmune diseases)
  • Receiving other experimental therapies that may affect oral or systemic inflammation
  • Pregnancy or lactation
  • Inability or unwillingness to provide informed consent
  • History of oral or periodontal surgery within the last 6 months affecting measurements

AI-Screening

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Trial Site Locations

Total: 2 locations

1

Clinical Emergency County Hospital Craiova

Craiova, Romania

Actively Recruiting

2

University of Medicine and Pharmacy of Craiova

Craiova, Romania

Actively Recruiting

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Research Team

P

Petra Surlin, Professor

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

3

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