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The Effects of Stainless Steel Crowns Applied With Hall Technique on Occlusal Vertical Dimension

Hall Teknik Ile Uygulanan Paslanmaz Celik kronların Okluzal Dikey Boyuta Etkilerinin değerlendirilmesi

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03010618
Enrollment
125
Registered
2017-01-05
Start date
2017-01-24
Completion date
2019-12-31
Last updated
2017-07-19

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Caries, Dental

Keywords

hall technique, stainless steel crowns, temporomandibular joint, dental caries, occlusion

Brief summary

In recent years restoring carious of fractured primary teeth with stainless steel crowns (SSC) has became more popular than ever. On the other hand the traditional operative approach of complete removal of caries is steadily losing support due to successful results with materials of high microleakage resistance. Treatment time and pain control in asymptomatic teeth has always been a problem in children. Hall technique is a minimally invasive treatment protocol that doesn't require local anesthesia, use of rotating devices for caries removal to restore primary teeth with SSC. But this protocol also raised questions in the scientific community about its possible effects on the dentition and temporomandibular joint (TMJ) for causing primary occlusal contact and increasing vertical dimension. The aim of our research is to study the effects of Hall technique's premature occlusal contact on TMJ.

Interventions

OTHERHall technique stainless steel crowns

Primary carious tooth will be treated with stainless steel crowns without local anesthesia or caries removal and the increase in the occlusal vertical dimension will be monitored in two subsequent appointments with measuring canine overbite.

Sponsors

Bezmialem Vakif University
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
5 Years to 8 Years
Healthy volunteers
Yes

Inclusion criteria

* No systemical illness * Willing to come to control appointments * No symptoms of pulpal inflammation * To have at least 1, 3 at most dentin caries primary teeth without infection, mobility, Angle class I profile and molar relation * Willing to participate the study

Exclusion criteria

* History of diagnosed systemic illness * Anterior/ posterior crossbite * Presence of dental pain * Root resorption exceeding 2/3's of the treated tooth * Gingival inflammation, periodontal disease * Signs of parafunctionism, bruxism * Facial asymmetry * Signs or symptoms of temporomandibular disfunction * Not willing to participate

Design outcomes

Primary

MeasureTime frameDescription
Complete canine overbite return30 daysThe length of overbite between upper and lower canines will be measured at beginning of the study with marking the overlapping contact point of the upper left canine and length of a straight line to the tip of the lower left canine will be recorded in mm with a standard WHO gingival probe. Full return to this level will be considered as Complete canine overbite return and failure to reach this level will in 30 days will require the patient to be scheduled for an extra recall in every 2 weeks until overbite returns to the pretreatment level.

Countries

Turkey (Türkiye)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026