Partial Edentulism Clinical Trial
Official title:
Improving Oral Health Function With Implant Supported Partial Dentures
NCT number | NCT02590861 |
Other study ID # | 1510M78701 |
Secondary ID | |
Status | Withdrawn |
Phase | N/A |
First received | |
Last updated | |
Start date | June 2016 |
Est. completion date | June 2019 |
Verified date | March 2019 |
Source | University of Minnesota - Clinical and Translational Science Institute |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
Distal extension Partial Removable Dental Prostheses (PRDPs) are less stable than tooth supported PRDPs due to progressive resorption of the alveolar ridge, which alters the retention and support generated by alveolar bone height. In addition, long-term wearers suffer with progressive alveolar ridge resorption that contributes to greater instability. The loss of stability and retention under the PRDP can lead to difficulties during mastication and swallowing, because of movement of the partial denture. These difficulties force patients to self-select food substances that are softer and easier to chew and possibly create changes in social eating. Therefore, having a partial denture that is poorly retentive will impact their oral health related quality of life Oral Health Related Quality of Life (OHRQoL). The placement of a dental implant into the edentulous area will transform a conventional PRDP into an Implant Supported PRDP, which will improve the functional capacity of partial denture wearers, especially their ability to comminute harder food substances such as fruits and nuts. The purpose of this study is to quantitatively measure the functional differences of patients wearing conventional PRDP with patients wearing implant supported PRDPs and Oral Health Impact of patients wearing implant supported PRDPs. The hypothesis is that patient wearing implant supported PRDPs will have greater functional capacity than patients wearing conventional PRDPs.
Status | Withdrawn |
Enrollment | 0 |
Est. completion date | June 2019 |
Est. primary completion date | December 2018 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 18 Years to 65 Years |
Eligibility |
Inclusion Criteria: - The inclusion criteria - posterior mandibular edentulism (on at least one side of the arch), - age 18-65, - general good health (self-reported), - a minimum of six mandibular anterior teeth remaining, - moderate to good periodontal health, - speak and read English at a high school level, - psychologically able to receive treatment. Exclusion Criteria: - The exclusion criteria - smokers, - poorly controlled diabetics, - untreated caries, - participants needing more than two crowns to support prosthesis, - symptomatic TMD, - cognitive impairment, - diagnosis of psychiatric disorder, - less than 25 mm interarch space, - lingual tori, - vertical bone height less than 10 mm, - Class II and Class III maxillomandibular relationship, - posterior bite collapse, - loss of vertical dimension, - Lekholm/Zarb grade C or more, - Lekholm/Zarb grade 3 or more, - the principle investigator decision. |
Country | Name | City | State |
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n/a |
Lead Sponsor | Collaborator |
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University of Minnesota - Clinical and Translational Science Institute |
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Cooper LF. The current and future treatment of edentulism. J Prosthodont. 2009 Feb;18(2):116-22. doi: 10.1111/j.1532-849X.2009.00441.x. Review. — View Citation
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Douglass CW, Watson AJ. Future needs for fixed and removable partial dentures in the United States. J Prosthet Dent. 2002 Jan;87(1):9-14. — View Citation
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* Note: There are 14 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | The number of participants with improved chewing function due to implant placement using Oral Health Impact Profile (OHIP) | The patient's chewing ability will be evaluated at 1-month, 2-month, 6-month, and 12-month recall appointments to evaluate patient satisfaction.The Oral Health Related Quality of life will be measured using the OHIP_14 instrument at the baseline, 1-month, 6-month, and 12-month recall appointment. | 1-month, 2-month, 6-month, and 12-month |
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