Specific occlusal scheme for patients with TM disorders

Specific occlusal scheme for partially edentulous patients with TM Disorders

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

ISRCTN

Registry ID

ISRCTN46870267

Enrollment

Registered

2017-11-10

Start date

2017-01-01

Completion date

Unknown

Last updated

2020-02-03

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

Conditions

Patients with problems in oro-facial function and temporo-mandibular disorders will be examined with respect to therapy with acrylic partial dentures for their lower jaws, applying specific occlusal scheme in artificial teeth of dentures Oral Health oro-facial function and temporo-mandibular disorders

Interventions

Treatment actions are related to occlusal corrections on masticatory-occlusal surfaces of artificial teeth in partial acrylic dentures, as well as composite restorations of incisal edges of anterior r

Zn-oxide eugenol paste Vomogal, Galenika, Serbia). The final mandibular impression will be taken using elastomer-silicone impression material (Oranwash, Zherrmack, Germany) and zinc oxide–eugenol impr

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: 1. Kennedy class II type of edentulous fields in the lower jaw, and edentulous upper jaw 2. Aged 46 and older

Exclusion criteria

Exclusion criteria: 1. Infectious diseases 2. Previous inabilities to wear partial dentures 3. Poor oral hygienic conditions

Design outcomes

Primary

Measure	Time frame
1. Dysfunctional problems and pain are measured using the pain questionnaires at the moment of preliminary impressing-starting time of phases of fabrication of dentures, at the moment of delivery of the dentures-baseline, after 3 months, after 6 months, after 9 months, after 12 months, after 24 months, after 36 months or after 48 months 2. Movements of the mandible is measured using millimetric ruler prior to preliminary impressing, and then at the moment of the delivery of the dentures-baseline, after 3 months, after 6 months, after 9 months, after 12 months, after 24 months, after 36 months or after 48 months 3. Occlusion of artificial teeth of acrylic partial lower dentures and complete upper dentures will be checked by conventional (two-sided) articulating paper are recorded as occlusal contacts on occlusal surfaces of teeth at the moment of delivery of dentures-baseline, after 3 months, after 6 months, after 9 months, after 12 months, after 24 months, after 36 months or after 48 months	—

Measure

Time frame

1. Dysfunctional problems and pain are measured using the pain questionnaires at the moment of preliminary impressing-starting time of phases of fabrication of dentures, at the moment of delivery of the dentures-baseline, after 3 months, after 6 months, after 9 months, after 12 months, after 24 months, after 36 months or after 48 months 2. Movements of the mandible is measured using millimetric ruler prior to preliminary impressing, and then at the moment of the delivery of the dentures-baseline, after 3 months, after 6 months, after 9 months, after 12 months, after 24 months, after 36 months or after 48 months 3. Occlusion of artificial teeth of acrylic partial lower dentures and complete upper dentures will be checked by conventional (two-sided) articulating paper are recorded as occlusal contacts on occlusal surfaces of teeth at the moment of delivery of dentures-baseline, after 3 months, after 6 months, after 9 months, after 12 months, after 24 months, after 36 months or after 48 months

—

Secondary

Measure	Time frame
There are no secondary outcome measures.	—

Countries

Serbia

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Feb 4, 2026