Association Between Periodontal Morphology and Non-Carious Cervical Lesions
NCCL-PM
Relationship Between Periodontal Morphology, Oral Habits, and Non-Carious Cervical Lesions: A Cross-Sectional Observational Study
1 other identifier
observational
180
1 country
1
Brief Summary
This observational study aims to investigate the relationship between periodontal morphology, oral hygiene habits, and non-carious cervical lesions (NCCLs) in adults aged 18-65 years. The main questions it aims to answer are: Is there an association between periodontal soft tissue characteristics and the presence of NCCLs? Are oral hygiene habits and parafunctional behaviors associated with NCCLs? Participants will: Complete a structured questionnaire about oral hygiene habits and oral behaviors Undergo a clinical periodontal examination including assessment of plaque index, gingival index, probing depth, gingival recession, keratinized tissue width, gingival phenotype, and NCCL presence on the maxillary first premolar tooth
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for all trials
Started Feb 2026
Shorter than P25 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
February 26, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
May 15, 2026
CompletedStudy Completion
Last participant's last visit for all outcomes
May 15, 2026
CompletedFirst Submitted
Initial submission to the registry
June 1, 2026
CompletedFirst Posted
Study publicly available on registry
June 5, 2026
CompletedJune 5, 2026
May 1, 2026
3 months
June 1, 2026
June 1, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Presence of Non-Carious Cervical Lesions
The presence or absence of non-carious cervical lesions on the maxillary first premolar tooth will be assessed by clinical examination. NCCL will be recorded as a binary outcome: present or absent.
At baseline / single clinical examination
Secondary Outcomes (3)
Keratinized Tissue Width
At baseline / single clinical examination
Gingival Phenotype
At baseline / single clinical examination
Oral Hygiene Habits
At baseline / single assessment
Study Arms (2)
NCCL Present
Participants presenting with non-carious cervical lesions on the maxillary first premolar tooth during clinical examination.
NCCL Absent
Participants without non-carious cervical lesions on the maxillary first premolar tooth during clinical examination.
Interventions
Clinical periodontal examination and questionnaire-based assessment will be performed to evaluate periodontal morphology, oral hygiene habits, and the presence of non-carious cervical lesions (NCCLs). Clinical parameters including probing depth, gingival recession, clinical attachment level, keratinized tissue width, gingival phenotype, plaque index, gingival index, dentin hypersensitivity, and tooth position will be recorded on the maxillary first premolar tooth. Participants will also complete a structured questionnaire regarding oral hygiene behaviors, toothbrushing habits, and parafunctional activities.
Eligibility Criteria
Adult patients attending the Faculties of Dentistry at Necmettin Erbakan University and Bilecik Seyh Edebali University for routine dental examination or periodontal evaluation will be recruited for this observational study. Participants will be selected from individuals presenting to the university dental clinics during the study period. The study population consists of community-based dental patients undergoing routine clinical periodontal assessment and questionnaire-based oral health evaluation.
You may qualify if:
- Adults aged between 18 and 65 years
- Presence of the maxillary first premolar tooth in the oral cavity
- Presence of at least 20 natural teeth
- Periodontally stable individuals without generalized active periodontal destruction
- Systemically healthy individuals or individuals with controlled systemic diseases
- Individuals who voluntarily agree to participate and provide informed consent
You may not qualify if:
- Presence of extensive restoration, caries, endodontic treatment, cervical restoration, crown/bridge restoration, orthodontic brackets, or retainers on the maxillary first premolar tooth
- Missing posterior teeth or edentulous posterior segments
- Ongoing orthodontic treatment
- Severe bruxism or use of occlusal splints/night guards
- Gastroesophageal reflux disease or bulimia nervosa
- Frequent acidic beverage consumption
- Smoking ≥5 cigarettes per day
- Pregnancy or lactation
- Individuals unable to comply with the clinical examination procedures
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Bilecik Seyh Edebali Universitesilead
- Necmettin Erbakan Universitycollaborator
Study Sites (1)
Bilecik Seyh Edebali University Faculty of Dentistry
Bilecik, Bilecik, 11100, Turkey (Türkiye)
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- observational
- Observational Model
- CASE CONTROL
- Time Perspective
- CROSS SECTIONAL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
June 1, 2026
First Posted
June 5, 2026
Study Start
February 26, 2026
Primary Completion
May 15, 2026
Study Completion
May 15, 2026
Last Updated
June 5, 2026
Record last verified: 2026-05
Data Sharing
- IPD Sharing
- Will not share