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Recruiting NCT07666360

NCT07666360 An Investigation of Cranio-Cervico-Mandibular Factors Predicting the Severity of Temporomandibular Disorders

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Clinical Trial Summary
NCT ID NCT07666360
Status Recruiting
Phase
Sponsor sevilay seda bas
Condition Temporomandibular Disorder
Study Type OBSERVATIONAL
Enrollment 60 participants
Start Date 2026-06-19
Primary Completion 2026-07-10

Eligibility & Interventions

Sex All sexes
Min Age 18 Years
Max Age 55 Years
Study Type OBSERVATIONAL
Interventions
Assessments

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

This is an observational study. You will not receive an experimental treatment; researchers will collect data based on your existing condition or standard treatment.

This trial targets 60 participants in total. It began in 2026-06-19 with a primary completion date of 2026-07-10.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

This cross-sectional study will examine the relationship between mandibular dysfunction, cervical joint position sense, craniovertebral angle, neck pain, and temporomandibular dysfunction (TMD) severity. TMD severity, mandibular function, cervical proprioception, craniovertebral angle, and neck pain history will be assessed using standardized clinical tools and questionnaires. The study will evaluate the associations between these variables and determine the factors that may predict TMD severity.

Eligibility Criteria

Inclusion Criteria: * Fonseca Anamnestic Index score \> 15 * aged 18 years and older Exclusion Criteria: * Received medical, orthodontic, or physiotherapy treatment targeting the temporomandibular joint and/or cervical region within the past six months * used analgesic, anti-inflammatory, or muscle relaxant medications * history of cervical spine or cranio-cervical surgery or major trauma * a history of facial or TMJ trauma, TMJ subluxation or dislocation * partial or complete dental prostheses * had missing teeth * neurological, rheumatological, or systemic inflammatory diseases

Contact & Investigator

Central Contact

Sevilay Seda BAŞ, PhD

✉ ssbas@aybu.edu.tr

📞 +90 (312) 906 1683

Frequently Asked Questions

Who can join the NCT07666360 clinical trial?

This trial is open to participants of all sexes, aged 18 Years or older, up to 55 Years, studying Temporomandibular Disorder. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT07666360 currently recruiting?

Yes, NCT07666360 is actively recruiting participants. Contact the research team at ssbas@aybu.edu.tr for enrollment information.

Where is the NCT07666360 trial being conducted?

This trial is being conducted at Ankara, Turkey (Türkiye).

Who is sponsoring the NCT07666360 clinical trial?

NCT07666360 is sponsored by sevilay seda bas. The trial plans to enroll 60 participants.

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ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: July 2026  ·  Data Methodology