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โ† Trials
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Patient Perception and Oral Function of Implant Restorations

RecruitingNAAges 30 Years - anyAllUniversity of Copenhagen
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In plain words

What the trial is, and whether it could suit you

The overall aim is to evaluate the patient-reported outcome and efficiency of replacing posterior teeth with implant-supported crowns compared to RDPs and no treatment. Sub-aims are to evaluate a new 3D-methods for registration of occlusion and to test two crown designs. Thus, the study design has three aims: * To analyze patient perception including OHRQoL, when missing posterior teeth are replaced with implant-supported crowns compared to removable dental prostheses (RDPs) or no replacement. * To develop and validate new 3D digital methods for assessing occlusal contacts between upper and lower jaw and to analyze the methods relation to masticatory ability and efficiency. * To compare the difference in biological technical outcomes between splinted and non-splinted implant-supported crowns over time.

Sign in to get the eligibility rules as simple questions to take to your doctor.

๐Ÿ“‹ Eligibility rules (as published)
Inclusion Criteria: * Partially edentulous subjects with missing posterior teeth (Kennedy class I or class II) in the upper or lower jaw, in need for fixed implant-supported crowns to replace the missing teeth are offered to be enrolled if they fulfill the following inclusion criteria. The participants must be in good health and with no contraindications for undergoing dento-alveolar surgery. Exclusion Criteria: * Untreated or active, progressive periodontitis * Intake of (high dose) antiresorptive medicine or earlier medication related osteonecrosis of the jaw * Therapeutic radiation to the head and neck * Uncontrolled diabetes or systemic corticosteroids * Heavy smoking (\>20 cigarettes/day) * An inability to open the mouth wide enough to place implants * Decayed or unrestored anterior/premolar teeth * Need for major bone augmentation (e.g., bone block graft, extensive augmentations with second operation for implant insertion) * \< 8 mm bone height to the alveolar nerve or sinus maxillaris * Parafunctional habits or untreated temporomandibular dysfunctions or orofacial pain * Unable to cooperate or too ill to complete the experiment * Lack of signed informed consent
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What it tests

  • Splinted
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Where

1 site
Faculty of Health and Medical Sciences
Copenhagen, Denmark
๐Ÿค Taking part is your choice, and you can leave at any time. Only the trial team can confirm you are eligible โ€” always decide together with your own doctor.
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