NCT07629492

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

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
180

participants targeted

Target at P50-P75 for all trials

Timeline
Completed

Started Feb 2026

Shorter than P25 for all trials

Geographic Reach
1 country

1 active site

Status
completed

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

Completed
3 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

May 15, 2026

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

May 15, 2026

Completed
17 days until next milestone

First Submitted

Initial submission to the registry

June 1, 2026

Completed
4 days until next milestone

First Posted

Study publicly available on registry

June 5, 2026

Completed
Last Updated

June 5, 2026

Status Verified

May 1, 2026

Enrollment Period

3 months

First QC Date

June 1, 2026

Last Update Submit

June 1, 2026

Conditions

Keywords

non carious cervical lesionperiodontal morphologyoral hygiene habits

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.

Diagnostic Test: Periodontal Examination and Oral Habit Assessment

NCCL Absent

Participants without non-carious cervical lesions on the maxillary first premolar tooth during clinical examination.

Diagnostic Test: Periodontal Examination and Oral Habit Assessment

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.

NCCL AbsentNCCL Present

Eligibility Criteria

Age18 Years - 65 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

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

Study Sites (1)

Bilecik Seyh Edebali University Faculty of Dentistry

Bilecik, Bilecik, 11100, Turkey (Türkiye)

Location

MeSH Terms

Conditions

Gingival Recession

Condition Hierarchy (Ancestors)

Gingival DiseasesPeriodontal DiseasesMouth DiseasesStomatognathic DiseasesPeriodontal Atrophy

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

Locations