Orofacial Pain Clinical Trial
Official title:
Neuro Occlusal Rehabilitation in Patient With Peripheral Facial Paralysis - a Randomized Clinical Trial
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 |
Verified date | November 2017 |
Source | Federal University of São Paulo |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
- 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.
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 |
Country | Name | City | State |
---|---|---|---|
Brazil | Federal University of São Paulo | São Paulo |
Lead Sponsor | Collaborator |
---|---|
Federal University of São Paulo |
Brazil,
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
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) |
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