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A cross-over randomised clinical trial of eccentric occlusion in complete dentures
被引:24
|作者:
Paleari, A. G.
[1
]
Marra, J.
Rodriguez, L. S.
[1
]
de Souza, R. F.
[2
]
Pero, A. C.
[1
]
Mollo, F. de A., Jr.
[1
]
Compagnoni, M. A.
[1
]
机构:
[1] Univ Estadual Paulista, Dept Dent Mat & Prosthodont, Araraquara Dent Sch, UNESP, BR-14801903 Araraquara, SP, Brazil
[2] Univ Sao Paulo, Dept Dent Mat & Prosthodont, Ribeirao Preto Dent Sch, USP, BR-14049 Ribeirao Preto, SP, Brazil
基金:
巴西圣保罗研究基金会;
关键词:
complete denture;
dental occlusion;
cross-over studies;
randomised controlled trial;
PATIENT SATISFACTION;
BALANCED OCCLUSION;
CANINE GUIDANCE;
QUALITY;
D O I:
10.1111/j.1365-2842.2012.02299.x
中图分类号:
R78 [口腔科学];
学科分类号:
1003 ;
摘要:
The objective of this study is to compare the effects of canine guidance (CG) and bilateral balanced occlusion (BBO) on denture satisfaction and kinesiographic parameters of complete denture wearers, by means of a cross-over trial. Fifty edentulous patients received new maxillary and mandibular complete dentures. After the intra-oral adjustments and adaptation period, 44 participants were enrolled in the trial and randomly received a sequence of occlusal schemes: BBO followed by CG, or CG followed by BBO. Outcomes were assessed after 30 days of each occlusal scheme. Participants answered a denture satisfaction questionnaire and a kinesiograph instrument recorded mandibular physiologic movements and pattern of maxillary denture movement during chewing. Wilcoxon test and paired sample t-test were used to compare satisfaction levels and kinesiographic data for each occlusal scheme, respectively (a = 0.05). The results showed no differences between occlusal schemes on participants satisfaction and in any of the kinesiographic parameters studied, except for the vertical intrusion of the maxillary complete denture during chewing, which was lower with CG. It can be concluded that the occlusal scheme did not influence on satisfaction and kinesiographic parameters evaluated, as long as volume and resilience of residual edentulous ridges of the participants were normal. Clinical Trial Registration Identifier: NC.T01420536.
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页码:615 / 622
页数:8
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