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Clinical Trials in Turkey / NCT06982898
Completed Not applicable

Digitalization of Maxillo-mandibular Relation for Arches With Occlusal Support Loss

NCT06982898 · tracked via the Priya Life Science Turkey tracker
Sponsor
Kıvanç Akça
Phase
Not applicable
Started
2025-05-01
Last updated
2026-09-28

Condition(s) studied

Prosthetic TreatmentOcclusal AnalysisDigitalism

Investigational drug(s) / intervention(s)

Fixed prosthesis with bimanual CR and intraoral scan

Fixed prosthesis with bimanual CR and intraoral scan: Tooth-supported fixed prostheses were fabricated using centric relation records obtained by two different methods: 1. Bimanual manipulation technique, with jaw relation records captured using an intraoral scanner. 2. Neuromuscular deprogramming technique, with jaw relation records obtained using a jaw movement tracking and analysis device.

Study summary

Accurate recording of the intermaxillary relationship is crucial for achieving successful restorative outcomes.

In cases of occlusal support loss, determining and recording the intermaxillary relationship becomes more complex.

This study aims to compare the occlusal compatibility of restorations fabricated using either an intraoral scanner or a jaw motion tracking and analysis device for recording the intermaxillary relationship in patients with occlusal support loss.

Eligibility

Sex
ALL
Min age
18 Years
Max age
65 Years
Healthy volunteers
Accepted
Inclusion Criteria: * Voluntary participation after reading and understanding the informed consent form. * Age between 18 and 65 years with completed growth and development. * Healthy dental and periodontal condition. * Presence of bilateral edentulism in the maxillary posterior region leading to occlusal support loss, requiring fixed prosthetic treatment. * Fixed dentition present in the mandible. Exclusion Criteria: * Refusal to voluntarily participate after reading the informed consent form. * General health condition unsuitable for prosthetic treatment. * Use of removable prostheses in the mandibular arch. * Presence of temporomandibular joint dysfunction, orofacial pain, or acute oral disease.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Hacettepe University, Faculty of Dentistry Ankara Turkey (Türkiye)

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06982898 on ClinicalTrials.gov ↗ ← All trials in Turkey