Biochemical Factors in Patients With and Without Bruxism
The Evaluation of Biochemical Factors in Bruxist and Non-Bruxist Patients: Case Control Study
1 other identifier
observational
60
1 country
1
Brief Summary
This observational case-control study aimed to compare biochemical factors related to calcium metabolism between adults with and without bruxism. Participants were classified into bruxism and control groups based on self-reported bruxism behaviors assessed using the BRUX Scale together with standardized clinical examination findings. Serum vitamin D, parathyroid hormone (PTH), calcium, albumin, and albumin-corrected calcium levels were evaluated and compared between the two groups. The study aimed to determine whether these biochemical parameters differ between individuals with and without bruxism and to provide further insight into their potential relationship with bruxism
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for all trials
Started May 2023
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
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
Study Start
First participant enrolled
May 1, 2023
CompletedPrimary Completion
Last participant's last visit for primary outcome
November 1, 2023
CompletedStudy Completion
Last participant's last visit for all outcomes
February 1, 2024
CompletedFirst Submitted
Initial submission to the registry
August 21, 2026
CompletedFirst Posted
Study publicly available on registry
August 25, 2026
CompletedAugust 25, 2026
August 1, 2026
6 months
August 21, 2026
August 21, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Serum Vitamin D,calcium,albumin and PTH level
Serum 25-hydroxyvitamin D \[25(OH)D\], calcium, PTH and albumin levels were obtained from available laboratory records and compared between participants with and without bruxism.
Within 6 months before study assessment
Study Arms (2)
Bruxism Group
Participants who met the predefined criteria for bruxism based on self-reported bruxism behaviors assessed using the BRUX Scale and standardized clinical examination findings
Control Grup
Participants who did not meet the predefined criteria for bruxism and were matched to the bruxism group according to age and sex.
Eligibility Criteria
The study population consisted of adults evaluated at the Department of Oral and Maxillofacial Surgery, Faculty of Dentistry, Ankara Yildirim Beyazit University. Eligible participants with suspected bruxism were assessed using self-reported bruxism behaviors and standardized clinical examination findings. Participants meeting the predefined criteria for bruxism constituted the bruxism group. Eligible participants without bruxism were selected as controls and matched to the bruxism group according to age and sex. Biochemical laboratory results available from the preceding 6 months were evaluated.
You may qualify if:
- Age 18 years or older. American Society of Anesthesiologists (ASA) physical status I or II. Availability of biochemical laboratory results, including serum vitamin D, parathyroid hormone (PTH), calcium, and albumin, obtained within the previous 6 months.
- Agreement to participate in the study.
You may not qualify if:
- Use of medications affecting vitamin D metabolism. Severe malocclusion. Complete or partial edentulism. Active dental or periodontal pain. History of jaw trauma. History of orthognathic surgery. History of temporomandibular joint (TMJ) surgery. Congenital craniofacial anomalies. Psychiatric disorders. Systemic diseases affecting bone metabolism.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Ankara Yıldırım Beyazıt University
Ankara, 06790, Turkey (Türkiye)
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- observational
- Observational Model
- CASE CONTROL
- Time Perspective
- RETROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
August 21, 2026
First Posted
August 25, 2026
Study Start
May 1, 2023
Primary Completion
November 1, 2023
Study Completion
February 1, 2024
Last Updated
August 25, 2026
Record last verified: 2026-08
Data Sharing
- IPD Sharing
- Will not share