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The effect of non-surgical periodontal therapy on clinical, microbiological, and biochemical parameters in individuals with gingivitis during puberty

The effect of non-surgical periodontal therapy on clinical, microbiological, and biochemical parameters in individuals with gingivitis during puberty

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
TCTR
Registry ID
TCTR20251125003
Enrollment
88
Registered
2025-11-25
Start date
2025-11-01
Completion date
Unknown
Last updated
2026-08-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Individuals in the pubertal period and post-pubertal period diagnosed with either, -Dental plaque-induced generalized gingivitis or, -Periodontal health Diagnosis made according to the criteria established in the 2017 World Workshop on the Classification of Periodontal and Peri-Implant Diseases and Conditions (Chapple et al., 2018) Gingivitis Non-surgical periodontal therapy Puberty

Interventions

This group will include individuals in the pubertal period with no clinical signs of periodontal inflammation (such as redness and/or edema in the gingiva), no radiographic bone loss, and no history o
Periodontally healthy group during puberty,Generalized gingivitis group during puberty,Periodontally healthy group post-puberty,Generalized gingivitis group post-puberty

Sponsors

Biruni University Scientific Research Projects
Lead Sponsor
The Scientific and Technological Research Council of Turkiye
Collaborator

Eligibility

Sex/Gender
All
Age
8 Years to 30 Years

Inclusion criteria

Inclusion criteria: 1. Diagnosed with periodontal health or dental plaque-induced generalized gingivitis according to the criteria established in the 2017 World Workshop on the Classification of Periodontal and Peri-Implant Diseases and Conditions (Chapple et al., 2018) 2. Age between 8 and 30 years 3. For individuals 19 years and younger, having a body mass index (BMI) between the 5th and 85th percentile 4. For individuals 20 years and older, having a BMI between 18.5 and 24.9 kg/m2 5. Willing to participate in the study

Exclusion criteria

Exclusion criteria: 1. Presence of any systemic condition or disease that may affect periodontal tissues 2. Use of medications that may influence periodontal tissues or hormonal balance (such as antihypertensives, antidiabetics, oral contraceptives, or hormone supplements) 3. Pregnancy or breastfeeding 4. Smoking 5. Undergoing orthodontic treatment 6. Receiving periodontal treatment within the last 3 months 7. Use of systemic antibiotics within the last 3 months

Design outcomes

Primary

MeasureTime frame
Changes in IL-1 beta levels in gingival crevicular fluid at baseline (T0), 6 weeks after treatment (T1), and 12 weeks after treatment (T2) ELISA essay,Gingival inflammation at baseline (T0), 6 weeks after treatment (T1), and 12 weeks after treatment (T2) Gingival index,Changes in IL-1 beta levels in saliva at baseline (T0), 6 weeks after treatment (T1), and 12 weeks after treatment (T2) ELISA essay

Secondary

MeasureTime frame
Changes in IL-6 levels in gingival crevicular fluid and saliva at baseline (T0), 6 weeks after treatment (T1), and 12 weeks after treatment (T2) ELISA essay,Changes in the Prevotella intermedia levels at baseline (T0), 6 weeks after treatment (T1), and 12 weeks after treatment (T2) digital PCR,Probing depth at baseline (T0), 6 weeks after treatment (T1), and 12 weeks after treatment (T2) Periodontal probe (mm)

Countries

Turkey

Contacts

Public ContactBurcu Karaduman

Biruni University, Faculty of Dentistry, Department of Periodontology

bkaraduman@biruni.edu.tr905323763366

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 10, 2026