Periodontitis Clinical Trials

Find Periodontitis Clinical Trials Near You

The Relationship of HALP Score, Blood-Based Inflammatory Indices, and Salivary MMP-8 Levels With Periodontal Disease and Healing After Non-Surgical Periodontal Therapy

Status: Recruiting
Location: See location...
Intervention Type: Procedure
Study Type: Observational
SUMMARY

This observational clinical study aims to investigate the relationship between the HALP score (Hemoglobin × Albumin × Lymphocyte / Platelet), several blood-based inflammatory indices (including NLR, PLR, LMR, and SII), and salivary MMP-8 levels in individuals with periodontal health, gingivitis, and stage III/IV periodontitis. The study also evaluates how these biomarkers relate to healing following non-surgical periodontal therapy. A total of 180 participants aged 18-65 years will be included: 50 healthy individuals, 50 patients with gingivitis, and 80 patients with stage III/IV periodontitis. All participants will undergo periodontal clinical examination and provide blood and saliva samples at baseline. Individuals in the gingivitis and periodontitis groups will receive standard non-surgical periodontal treatment (full-mouth debridement) and will return for a 3-month follow-up visit, where periodontal measurements will be repeated. In the periodontitis group, an additional blood sample will be collected at the 3-month follow-up visit. The primary objective is to determine whether baseline HALP score, systemic inflammatory indices, and salivary MMP-8 levels differ between participants who show good versus poor healing after treatment. Secondary objective include comparing biomarker levels across periodontal status groups. The findings may contribute to early prediction of treatment response and personalized periodontal care.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 65
Healthy Volunteers: t
View:

• Adults aged 18-65 years

• Ability to provide informed consent

• No systemic diseases or conditions affecting periodontal status

• For Healthy Group: Probing depth ≤3 mm, no attachment loss, no radiographic bone loss

• For Gingivitis Group: Gingival inflammation and bleeding on probing without attachment loss or bone loss

• For Periodontitis Group: Stage III or stage IV periodontitis according to 2018 classification

• No periodontal treatment within the past 6 months

• Willingness to attend follow-up visits

Locations
Other Locations
Turkey
Erzincan Binali Yıldırım University Faculty of Dentistry
RECRUITING
Merkez
Contact Information
Primary
Ömer Faruk Okumuş, Assistant Professor
okumus.omer24@gmail.com
+905532140969
Time Frame
Start Date: 2025-11-25
Estimated Completion Date: 2026-11-25
Participants
Target number of participants: 180
Treatments
Periodontally Healthy Individuals
Participants with no clinical signs of gingival inflammation, probing depth ≤3 mm, no clinical attachment loss, and no radiographic bone loss. These individuals serve as the healthy control group.
Gingivitis Patients
Participants with visible signs of gingival inflammation and bleeding on probing, but without clinical attachment loss or radiographic bone loss. These individuals will receive standard non-surgical periodontal therapy.
Stage III/IV Periodontitis Patients
Participants diagnosed with stage III or stage IV periodontitis, characterized by clinical attachment loss, probing depth ≥5 mm, and radiographic bone loss. These individuals will receive standard non-surgical periodontal therapy and will be re-evaluated at 3 months.
Related Therapeutic Areas
Sponsors
Collaborators: Erzincan Binali Yildirim Universitesi
Leads: Ömer Faruk Okumuş

This content was sourced from clinicaltrials.gov