Clinical Trials Logo

Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01327157
Other study ID # CEP 0323/08
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date March 2009
Est. completion date March 2010

Study information

Verified date November 2017
Source Federal University of São Paulo
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

- The purpose of this study was to evaluate the effects of Neuro Occlusal Rehabilitation (RNO) in patients with peripheral facial palsy (PFP) disease, noting the decrease in symptoms of masticatory dysfunction.

- According to Carvalho (2009) patients with PFP have chronic unilateral masticatory preference. Santos et al. (2009) in the same year noted that these conditions can lead to problems with temporomandibular disorder.

- Hypothesis- known that performing occlusal adjustment in these patients with chronic PFP, ensuring a maximum of dental contacts and a final stop of the masticatory cycle stable, providing a balanced occlusion.

- dental cleaning was performed in two groups for the blind study

- visual analog scale -To assess the quality of the oral functions of these patients, the investigators applied the visual analog scale(VAS) and statistically evaluated the degree of satisfaction regarding the functions of oro facial in relation to mastication and temporomandibular dysfunction.

- gnathostatic models were made in the treatment group in the first and last query.

- occlusal adjustment in treatment group.In the group treated occlusal adjustment was made in the teeth and applied a new (VAS) before and after treatment.

The RNO, is defined as a part of medicine that operates in stomatology occlusal plane as a guide to a harmonious development of the face, chewing facilitating bilateral and alternating. (Planas, 1997). It works through selective grinding on the occlusal platform, providing an increased number of dental contacts.


Description:

Purpose: To evaluate the effects of the Neuro-Rehabilitation occlusion in patients with chronic facial palsy by observing the decrease of the symptoms of masticatory dysfunction.

Methods: a selection of sixty-five patients with facial palsy (PFP 65) and idiopathic chronic trauma of the Otorhinolaryngology sector facial nerve disorders at UNIFESP.

Patients were of both genders, aged between 18 and 60. They were analyzed according to the criteria of inclusion and exclusion, resulting in forty-three patients.

However, due to problems inherent in research, a group of fourteen patients were randomized (sub-divided) into two groups: control and treatment.

The visual analog scale was used at the first consultation to patients in the control and treatment group.

All patients underwent a dental cleaning in order to blind the study. Seven patients belonged to the control group for three months per sequence, the VAS was performed in both groups. The control group was later reunited with the treatment group after three months of control period, increasing the number of patients who were examined in extracts, with similar features in a prognostic factor.

- Control group

- First visit- visual analogue scale and dental cleaning - Day 1

- Second visit, after a month, a new visual analog scale. Day-30

- Third-visit -one months after a new visual analogue scale Day 60 patient was a three visits with an interval of one month, performing a repeat procedure.

- Last visit - Day 90 visual analogue scale

- Treatment group The researchers applied the technique of Rehabilitation and Neuro Occlusal gnathostatic models that were made before and after treatment to count the dental contacts.

- First query - visual analogue scale and dental cleaning, preparation of initial models gnatostaticos and intervention- Day 1

- Second-query-after a month, a new visual analogue and intervention. Day 30

- Third query- -after a month, a new visual analogue and intervention Day 60

- Last query -after a month a new visual analogue scale and making models gnathostatic finals. Day 90 The treatment group had one month to see changes in oral functions, but for estatistic effects was computed only de first andy the last visit the number of the dental contact and the VAS. Day 90 Upon completion of the study patients continued to receive care in the ambulatory clinic of the university, but the attendance for this research was terminated.


Recruitment information / eligibility

Status Completed
Enrollment 14
Est. completion date March 2010
Est. primary completion date March 2010
Accepts healthy volunteers No
Gender All
Age group 18 Years to 60 Years
Eligibility Inclusion Criteria:

- patients with PFP over six months of treatment

- indentations

- carrier fixed partial dentures and removable drives and/or dental implants

- palsy classified as Grade III according to House and Brackmann scale

Exclusion Criteria:

- patients who already had other diseases in the region of the jaws before facial paralysis

- is toothless from installing, using or not dentures

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
occlusal adjustment.
It prompted the patient to perform the act of swallowing for 3 times to reach a terminal axis of rotation of the jaw and from this to start. Will be held palpation of the muscles, masseter and temporal on both sides and compared with the marks of carbon found in the teeth. After starts the adjustment following the rules of Guichet with a cylindrical drill with a thin cut . basic principles 1 Occlusive stress maximum distribution in centric relation 2 The occlusive strengths should by the teeth's major axis.3 When the contact is surface to surface, it must be exchanged to another surface point. 4 Once the stability to the centric relation is achieved, it should be kept. The rules to guide the occlusal adjustment selective grinding .
Behavioral:
Visual analog scale.
Visual analog scale-Graduation was held on the visual analogue scale in the first and last query to measure discomfort chewing.Graduation was held on the visual analogue scale .in the first and last query to measure discomfort chewing. After graduating dental cleaning was performed, with the purpose of blinding the study, Dental Cleaning.With engine using low speed, brushes, and prophylactic paste is carried out dental cleaning in the teeth of all patient. Dental Cleaning.With engine using low speed, brushes, and prophylactic paste is carried out dental cleaning in the teeth of all patient.

Locations

Country Name City State
Brazil Federal University of São Paulo São Paulo

Sponsors (1)

Lead Sponsor Collaborator
Federal University of São Paulo

Country where clinical trial is conducted

Brazil, 

References & Publications (5)

Christensen LV, Radue JT. Lateral preference in mastication: an electromyographic study. J Oral Rehabil. 1985 Sep;12(5):429-34. — View Citation

Martin E. [Neuro-occlusal rehabilitation and selective grinding: results after 1 year]. Orthod Fr. 2000 Jan;71(1):57-60. French. — View Citation

Planas M. [Neuro-occlusal rehabilitation: NOR]. Orthod Fr. 1971;42:333-47. French. — View Citation

Planas P. [Equilibrium and neuro-occlusal rehabilitation]. Orthod Fr. 1992;63 Pt 2:435-41. French. — View Citation

Rahal A, Goffi-Gomez MV. Clinical and electromyographic study of lateral preference in mastication in patients with longstanding peripheral facial paralysis. Int J Orofacial Myology. 2009 Nov;35:19-32. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Other Correlation Between the Increase of the Number of Dental Contact Points and the Improvement in the Subjective Evaluation Measured Through the Visual Analogic Scale . The correlation between the increase of the number of the dental contacts and the VAS evaluation final result from chronic peripheral facial paralysis patients, according to control and treated groups by the neuro occlusal rehabilitation technic. Day 01 and after 90 days of treatment (Day 180 for Treatment participants first receiving Placebo)
Other Correlation Between the Increase of the Number of Dental Contact Points and the Improvement in the Subjective Evaluation Measured Through the Visual Analogic Scale Whithout the Outlier. The correlation between the increase of the number of the dental contacts and VAS evaluation final result from chronic peripheral facial paralysis patients.
On this measure was excluded one outlier patient whose facial paralysis appeared in her childhood.
Observing the outlier patient, it was carried out a new scatterplot, ignoring her.
Day 01 and after 90 days of treatment (Day 180 for Treatment participants first receiving Placebo)
Primary The Visual Analog Scale for Pain Was Used to Grade Discomfort in Chewing After the Installation of Facial Paralysis. Level Zero is the Lack of Discomfort and 10 is the Maximum Degree of Discomfort. It is a scale-shaped ruler, which is associated with faces used to grade the degree of pain for patients, before and after treatments, or just graduating pain and its severity for the patient (Souza, 2002).
Patients were asked to fill the VAS with the following questions.
Do you chew well?
How would you classify your chewing at the moment?
If you have no trouble chewing, the rating is zero.
If you have any discomfort when you chew, your reference level is five.
If the discomfort is intense, its reference level is ten. The greater the discomfort, the greater the scale.
Day 1 (Day 91 for Treatment participants first receiving Placebo)
Primary Brand Carbon Count on Gnathostats Models Only in the treatment group were done gnatostatic models.The models were placed occluding brought with carbon, using the willis compass to keep occluding the posterior base of the model which are aligned with the rear. A model of the teeth was made to measure the occlusion of the teeth (i.e., the amount of contact between the upper and lower mandibles), and used carbon to count the the number of dental contacts, through the brand carbon made on the model, The dental contacts were counted in the models before and after treatment. The models are made in the first and last query. Day 01 and after 90 days of treatment (Day 180 for Treatment participants first receiving Placebo)
Secondary Visual Analog Scale It is a scale-shaped ruler, which is associated with faces used to grade the degree of pain for patients, before and after treatments, or just graduating pain and its severity for the patient (Souza, 2002).
Patients were asked to fill the VAS with the following questions. Do you chew well? How would you classify your chewing at the moment? If you have no trouble chewing, the rating is zero. If you have any discomfort when you chew, your reference level is five. If the discomfort is intense, its reference level is ten. The greater the discomfort, the greater the scale.
After 90 days of treatment (Day 180 for Treatment participants first receiving Placebo)
See also
  Status Clinical Trial Phase
Recruiting NCT04977349 - Manual Therapy Effectivity and Exercises in Musicians N/A
Recruiting NCT05584384 - The Use of tDCS in the Orofacial Pain N/A
Completed NCT00067366 - Brief Treatment for Temporomandibular Pain N/A
Completed NCT06132594 - Computed Guided Prolotherapy Versus Conventional Prolotherapy N/A
Not yet recruiting NCT03702101 - Detecting Auricular Points in OFP by a Novel APD ( APD-OFP)
Not yet recruiting NCT06065969 - Photobiomodulation Dosimetry s in Patients With Orofacial Pain N/A
Completed NCT04352881 - Evaluation of Out of Hours Dental Emergency Treatments
Not yet recruiting NCT04765007 - Efficacy of Mindfulness Therapy in Orofacial Chronic Pain N/A
Terminated NCT01883245 - Effects of Transcranial Direct Current Stimulation (tDCS) on Patients With Chronic Orofacial Pain Phase 2
Completed NCT00899717 - Occlusal Adjustment as Treatment for Chronic Orofacial Pain Phase 1/Phase 2
Recruiting NCT05430776 - Laser Therapy on Tension-type Cephalea and Orofacial Pain in Post-covid-19 Patients N/A
Active, not recruiting NCT03710967 - Bilateral TMS vs. Unilateral TMS N/A
Recruiting NCT04694274 - Genetic Polymorphisms and Their Association With Temporomandibular Disorders
Enrolling by invitation NCT06405646 - Concentration of Receptors With Affinity for Cannabidiol and Cannabinol and the Effect on Chronic Orofacial Pain of Muscle Origin
Not yet recruiting NCT05961501 - The Effectiveness of CBD and CBN in the Treatment of Facial Pain and Headache of Muscular Origin Phase 2/Phase 3
Completed NCT01949064 - Use of Electromyography With Bio-Feedback for the Treatment of Craniomandibular Disorders Phase 2
Recruiting NCT05562635 - CBD (Cannabidiol) Intraoral Application and TMD (Temporomandibular Disorders) Phase 2/Phase 3
Completed NCT04524806 - Influence of Stabilization Splint Thickness on The Temporomandibular Disorders N/A
Completed NCT03221946 - A Comparative Evaluation of Diclofenac Sodium Transdermal Patch, Oral Diclofenac Sodium With Intramuscular Injections of Diclofenac Sodium in Patients Suffering From Oral Pain Phase 4
Completed NCT04612855 - Post-traumatic Neuropathy of the Trigeminal Nerve