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Evaluation of adults that gnash their teeth before and after using appliance

Evaluation of the effect of occlusal splint use on the bite force, quality of sleep and salivary cortisol levels in subjects with sleep bruxism

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-3nkwyv
Enrollment
Unknown
Registered
2016-07-14
Start date
2015-02-01
Completion date
Unknown
Last updated
2025-10-27

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

Conditions

Bruxism

Interventions

- Dental decay
- Use of orthodontic braces
- Use of dentures (partial fixed or removable)
- Presence of dental implants in the molar region
The study will comprise 45 adults aged between 20 and 40 years, of both genders, students or employees of the University Community of the Region of Chapecó (Unochapecó) , Brazil , which will compose t
the conditions of the lips, gums, tongue, palate, buccal mucosa, labial and lingual brakes and present and absent teeth will be assessed. The following exclusion criteria will be considered (Rossetti,
- Abnormalities in soft tissues
- Pain of dental origin
- Periodontitis (presence of periodontal pockets and commitment of supporting tissues)
- Moderate to severe malocclusions diagnosed by the Orthodontic Treatment Need Index (IOTN - Index of Orthodontic Treatment Need) - Dental Component (Dental Health Component). This index is based on t
Device
Genetics
E06.520
C07.793.099

Sponsors

Faculdade de Odontologia de Piracicaba (UNICAMP)
Lead Sponsor
Universidade Federal de São Paulo (UNIFESP)
Collaborator

Eligibility

Age
20 Years to 40 Years

Inclusion criteria

Inclusion criteria: Adults; age ranging from 20 to 40 years; Caucasians; students or employees of the Universidade Comunitária da Região de Chapecó (Chapecó, Brazil).

Exclusion criteria

Exclusion criteria: Systemic disturbances which could compromise the evaluation of the stomatognathic system; neurological disorders; epilepsy; cerebral palsy; presence of systemic diseases or medication use that could interfere with muscle or salivary activity directly or indirectly; hypertension; cancer; rheumatoid arthritis; diabetes; dyslipidemia; xerostomia; use of antihistamine; use of benzodiazepines; use of antidepressants; use of anxiolytics; use of syrups; use of anti-inflammatory; use of corticoids; use of homeopathy; inappropriate behavior and/or refusal to cooperate in dental procedures and evaluation of the proposed variables.

Design outcomes

Primary

MeasureTime frame
Alterations on cortisol secretion after two months using occlusal splints, which will be quantifyed in saliva and analysed using inferential statistics with before and after-treatment results.;Improvement on bite force magnitude after two months using occlusal splints, which will be measured by gnathodynamometer and inferential statistics with before and after-treatment results.;Improvement on sleep quality after two months using occlusal splints, which will be analysed by a validated questionnaire and inferential statistics with before and after-treatment results.

Secondary

MeasureTime frame
Remission of signs and symptoms of TMD after two months using occlusal splints, verified by a validated protocol (RDC-TMD) and inferential analysis comparing before and after results.

Countries

Brazil

Contacts

Public ContactPaula;Paula Castelo;Castelo

Universidade Federal de São Paulo (UNIFESP);Universidade Federal de São Paulo (UNIFESP)

pcastelo@yahoo.com;pcastelo@yahoo.com11982024569;+55(11)3385 4137

Outcome results

None listed

Source: REBEC (via WHO ICTRP)