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NCT Number: NCT07491848

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

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.

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Key information

About this study

Periodontal disease is characterized by chronic inflammation and destruction of tooth-supporting tissues. Emerging evidence links oral inflammatory conditions with systemic diseases, forming the basis of periodontal medicine. Hepatitis B+D infection is associated with systemic inflammation and immune dysregulation, yet little is known about its impact on oral health and inflammatory mediators in oral fluids.

This prospective, observational case-control study will recruit adult participants from the University of Medicine and Pharmacy of Craiova. Participants will be divided into three groups:

Hepatitis B+D - Bulevirtide: Patients receiving bulevirtide therapy.

Hepatitis B+D - No Bulevirtide: Patients not receiving bulevirtide.

Healthy Controls: Systemically healthy adults.

Clinical oral-periodontal examinations will be performed by a specialist periodontist, with photographs documenting oral findings. Saliva and gingival crevicular fluid will be collected using non-invasive methods to measure targeted inflammatory biomarkers. Biological samples will be analyzed at the Immunology Laboratory of the University of Medicine and Pharmacy of Craiova and at the University of Amsterdam.

Assessments will be performed at baseline and 6 months. Relevant clinical data will be extracted from medical records following data protection regulations. Statistical analysis will evaluate associations between periodontal inflammation, oral biomarkers, and hepatitis B+D status, as well as the potential impact of bulevirtide therapy.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Adults (≥18 years old) capable of providing informed consent.
  • For Hepatitis B+D groups: confirmed hepatitis B and D co-infection.
  • Bulevirtide group: receiving bulevirtide therapy as prescribed.
  • No Bulevirtide group: not receiving bulevirtide.
  • For Healthy Control group: systemically healthy adults without hepatitis B or D infection.
  • Willingness to undergo oral-periodontal examination, saliva and gingival crevicular fluid collection, and oral cavity photography.

Exclusion criteria

  • Patients with other systemic diseases that could influence periodontal health (e.g., uncontrolled diabetes, autoimmune diseases).
  • Patients currently 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 that could affect measurements.

Treatment and study plan

Bulevirtide

Drug

Bulevirtide is an entry inhibitor used for the treatment of hepatitis B and D virus co-infection. In this observational study, patients receiving bulevirtide therapy as part of their routine clinical care will be evaluated for oral-periodontal clinical parameters and inflammatory biomarkers in saliva and gingival crevicular fluid.

No intervention

Other

Patients diagnosed with hepatitis B+D who are not receiving bulevirtide therapy and are evaluated for comparison of oral-periodontal parameters and biomarkers.

Primary outcomes

  1. Salivary inflammatory biomarker levels

    Time frame: Baseline and 6 months after initiation of treatment

    Quantitative assessment (pg/mL) of selected inflammatory biomarkers (e.g., IL-1β, IL-6, TNF-α) in saliva samples collected from participants in all study groups to evaluate the association between periodontal inflammation, hepatitis B+D infection, and bulevirtide treatment.

  2. Gingival crevicular fluid inflammatory biomarker levels

    Time frame: Baseline and 6 months

    Measurement (pg/mL) of targeted inflammatory mediators (e.g., IL-1β, IL-6, TNF-α) in gingival crevicular fluid samples to assess local periodontal inflammation and its relationship with hepatitis B+D infection and bulevirtide therapy.

Secondary outcomes

  1. Probing Depth (PD)

    Time frame: Baseline and 6 months

    Measurement of periodontal probing depth (in millimeters) at six sites per tooth to assess periodontal status in all study groups.

  2. Clinical Attachment Level (CAL)

    Time frame: Baseline and 6 months

    Assessment of clinical attachment level (in millimeters) to evaluate periodontal tissue destruction.

  3. Bleeding on Probing (BOP)

    Time frame: Baseline and 6 months

    Percentage of sites exhibiting bleeding on probing as an indicator of gingival inflammation.

  4. Plaque Index (PI)

    Time frame: Baseline and 6 months

    Assessment of dental plaque accumulation using a standardized plaque index score.

Study contacts

Contact information is provided by the study sponsor or research team.

Petra Surlin, Professor

CONTACT

[email protected]

0040745538483

Sponsors and collaborators

Lead sponsor

Research Center of Periodontal-Systemic Interactions

Other

Collaborators

  • Spitalul clinic judetean de urgenta Craiova
  • University of Medicine and Pharmacy Craiova

Registry information

Official study title

Oral-Periodontal Evaluation and Assessment of Biomarkers in Oral Fluids in Patients With Hepatitis B+D Treated With Bulevirtide

Important dates

Study start
2026
Primary completion
2027
Study completion
2027
First posted
Mar 25, 2026
Registry last updated
Mar 25, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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