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Salivary Stress Markers Associated With Malocclusion Severity

R

Recep Tayyip Erdogan University Training and Research Hospital

Status

Not yet enrolling

Conditions

Malocclusion

Study type

Observational

Funder types

Other

Identifiers

NCT07116317
ortho04/2025

Details and patient eligibility

About

The aim of this observational study is to evaluate the relationship between the severity of orthodontic malocclusion and psychophysiological stress levels in individuals aged 12 to 18 years. The study will investigate the association between malocclusion severity and both stress-related salivary biomarkers and psychosocial factors.

The primary research question is as follows:

As the severity of orthodontic malocclusion increases, do levels of salivary stress biomarkers (cortisol, DHEA, and chromogranin A), self-esteem, and social appearance anxiety significantly change in adolescent individuals?

Method:

The study will include participants between the ages of 12 and 18. The severity of malocclusion will be assessed through clinical examination. Psychological assessments will be conducted using structured questionnaires to measure self-esteem and social appearance anxiety. In addition, saliva samples collected in the morning will be analyzed using the ELISA method to determine levels of cortisol, DHEA, and chromogranin A (CgA). The data will be statistically analyzed to identify the potential relationship between orthodontic malocclusion and biological and psychosocial indicators of stress.

Enrollment

120 estimated patients

Sex

All

Ages

12 to 18 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients between the ages of 12 and 18,
  • Patients with all permanent teeth,
  • Patients with the ability to read and understand,
  • Patients with a cephalometric evaluation file and maxillary and mandibular impression dental models before diagnostic orthodontic treatment.

Exclusion criteria

  • Presence of any congenital craniofacial deformity (cleft lip and palate or any other craniofacial syndrome or deformity),
  • Patients who have previously initiated or completed orthodontic treatment,
  • Patients with a history of psychiatric illness, the presence of caries, facial asymmetry, and any skin deformity affecting facial aesthetics.

Trial design

120 participants in 4 patient groups

Patients with normal or minor malocclusion
Description:
Patients with a Dental Aesthetic Index score of ≤25
Patients with moderate malocclusion
Description:
Patients with a Dental Aesthetic Index score of 26-30
Patients with severe malocclusion
Description:
Patients with a Dental Aesthetic Index score of 31-35
Patients with obstructive malocclusion
Description:
Patients with a Dental Aesthetic Index score of ≥36

Trial contacts and locations

1

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Central trial contact

Tuba KOSE, Assistant Professor; Oguz KOSE, Professor Dr.

Data sourced from clinicaltrials.gov

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