Supplementary Implants Supporting Conventional Removable Dental Prosthesis (RDPs) in Kennedy Class I

  • STATUS
    Recruiting
  • End date
    Feb 28, 2025
  • participants needed
    20
  • sponsor
    University Hospital, Basel, Switzerland
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Updated on 19 February 2024
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Summary

In this study the additional effect of supplementary implants in patients with Kennedy Class I in terms of patient-reported outcome measures (PROMs) and cost-benefit-analyses comparing costs of maintenance care will be investigated

Details
Condition Partial Edentulism Kennedy Class 1
Age 18-100 years
Treatment dental implants and retentive implant components, dental implants and supportive implant components
Clinical Study IdentifierNCT04276246
SponsorUniversity Hospital, Basel, Switzerland
Last Modified on19 February 2024

Eligibility

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Inclusion Criteria

Subjects must have voluntarily signed the informed consent before any study action, are willing and able to attend scheduled follow-up visits, and agree that the encoded data will be collected and analyzed
Males and females with at least 18 years of age
intraoral situation with bilateral edentulous areas located posterior to the remaining natural teeth (Kennedy class I) in the upper or lower jaw
remaining dentition includes a first premolar, canine or incisor as the most posterior tooth

Exclusion Criteria

Uncontrolled systemic disease that would interfere with dental implant therapy
Patients who smoke > 10 cigarettes per day or tobacco equivalents
Patients with alcohol and/or drug abuse
Patients with chronic pain
Patients with untreated periodontitis and / or inadequate oral hygiene (Plaque Index < 30%)
Medical conditions requiring chronic high dose steroid therapy or anti-resorptive treatment
Conditions or circumstances, in the opinion of the investigators, which would prevent completion of study participation or interfere with analysis of study results such as history of non-compliance or unreliability
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Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.

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If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

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Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

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