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Recruiting Not applicable

Surfactant Protein D Levels in GCF Before and After MINST in Periodontitis

NCT07599657 · tracked via the Priya Life Science Egypt tracker
Phase
Not applicable
Started
2026-05-14
Last updated
2026-05-20

Condition(s) studied

PeriodontitisPeriodontitis Stage IIPeriodontitis Stage III

Investigational drug(s) / intervention(s)

Minimally Invasive Non-Surgical Periodontal Therapy

Minimally Invasive Non-Surgical Periodontal Therapy: Minimally invasive non-surgical periodontal therapy will include oral hygiene instructions, supragingival plaque control, and subgingival instrumentation using fine periodontal instruments, miniature Gracey curettes, thin ultrasonic tips, magnification when available, and local anesthesia when needed. Debridement will be performed for periodontal pockets while minimizing trauma to the soft tissues.

Study summary

This study will evaluate changes in Surfactant Protein D (SP-D) levels in gingival crevicular fluid (GCF) of patients with periodontitis before and after minimally invasive non-surgical periodontal therapy (MINST).

Participants diagnosed with stage II or III periodontitis will receive minimally invasive non-surgical periodontal treatment. GCF samples will be collected at baseline and 6 months after treatment, and SP-D levels will be measured using enzyme-linked immunosorbent assay (ELISA).

The study will also assess clinical periodontal outcomes, including full-mouth plaque score, full-mouth bleeding score, probing pocket depth, clinical attachment level, gingival recession, and patient satisfaction. Each participant will serve as their own control by comparing baseline values with 6-month post-treatment values.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Male and female participants aged 18 years or older. * Diagnosis of periodontitis, classified as stage II or stage III according to the 2018 classification system. * Presence of at least one tooth with probing pocket depth (PPD) of 5 mm or more, clinical attachment loss (CAL), and radiographic evidence of bone loss. * Presence of at least one intrabony defect with a radiographic intrabony component measuring 3 mm or more. Exclusion Criteria: * Current smokers or individuals with a history of smoking within the past year. * Pregnant or lactating women. * Use of systemic antibiotics or anti-inflammatory medications within the last 3 months. * Known allergy to any materials or agents used during periodontal therapy.

Primary outcome measure(s)

  • Change in Surfactant Protein D (SP-D) Levels in Gingival Crevicular Fluid — Baseline and 6 months after treatment
    Change in Surfactant Protein D (SP-D) concentration in gingival crevicular fluid from baseline to 6 months after minimally invasive non-surgical periodontal therapy. SP-D levels will be measured using enzyme-linked immunosorbent assay (ELISA) and reported in ng/mL.

Trial sites (1)

FacilityCityRegionStatus
Faculty of Dentistry, Cairo University Cairo Egypt Recruiting
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07599657 on ClinicalTrials.gov ↗ ← All trials in Egypt