Conventionally vs. Digitally Fabricated Complete Dentures: Clinical Treatment Outcome Differences

Sponsor
University of North Carolina, Chapel Hill (Other)
Overall Status
Withdrawn
CT.gov ID
NCT02521935
Collaborator
Global Dental Science, LLC (Other)
0
1
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36
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Study Details

Study Description

Brief Summary

Purpose: To compare complete denture outcomes between conventional and digital denture fabrication processes.

Participants: Sixteen edentulous adult patients in the University of North Carolina School of Dentistry Student Clinic who are seeking removable complete dentures.

Procedures (methods): Two complete sets of dentures will be fabricated for each subject: one using the conventional process (A) and the other using a digital process (B). Variability will be assessed by the research team, the treating dental students, an independent prosthodontist, and the patients through quantitative measures. Case selection and results analysis will be evaluated with recognition of the Prosthodontic Diagnostic Index.

Condition or Disease Intervention/Treatment Phase
  • Device: Complete traditional dentures
  • Device: Complete CADCAM dentures
N/A

Detailed Description

Rationale for Study Design An AB/BA (conventional=A, digital=B) crossover design with no wash-out period is flawed for this study, and its weakness is the potential for a carryover effect (benefits or risks associated with treatment A carry over to treatment B). A wash-out period is not feasible for this study because it would require the patient-subjects to suspend use of their dentures for the duration of the wash-out period.

The Investigators have decided to conduct the study using the ABB/BAA crossover design, which does not require a wash-out period and will permit testing and discounting of a possible carryover effect. In addition, this design is more appropriate for a small sample size than the AB/BA design.

The investigators are adding to the scant literature on digital dentures, information that has never before been studied - the retention, aesthetics, and stability of digital dentures compared to conventional dentures. Additionally, the investigators will have longitudinal data on these characteristics regarding digital dentures.

If the Functional Assessment of Dentures (FAD) and the patient evaluation show positive results for the digital dentures, this could lead to increased use of the Computer -Aided Design/ Computer -Aided Manufacturing (CADCAM) fabrication method which, in turn, would allow greater numbers of people to benefit from the advantages of the digital dentures as described earlier in this application (e.g., a better fit, fewer visits with less time in the chair, less biofilm formation, etc.)

Study Design

Study Type:
Interventional
Actual Enrollment :
0 participants
Allocation:
Randomized
Intervention Model:
Crossover Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Conventionally vs. Digitally Fabricated Complete Dentures: Clinical Treatment Outcome Differences
Study Start Date :
Jan 1, 2017
Anticipated Primary Completion Date :
Jan 1, 2018
Anticipated Study Completion Date :
Jan 1, 2020

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: Complete traditional dentures

Complete maxillary/mandible dentures made in the traditional manner.

Device: Complete traditional dentures
Arm 1-Standard Treatment Sequence for Traditional Removable Dentures in a Dental School Clinic (9 Appointments): Appointment 1: Examination & diagnosis & initial impressions. Appointment 2: Secondary impressions. Appointment 3: Secondary or definitive impressions (Often 2 appointments are needed to border mold and impression) Appointment 4: Maxillo-mandibular jaw relation records (both centric and vertical relation). Tooth selection. Appointment 5: Wax-trial denture try-in. Appointment 6: Insertion and instructions for care of definitive prostheses. Appointments 7-9 Post adjustments
Other Names:
  • complete conventional dentures
  • Active Comparator: Complete CADCAM dentures

    Complete maxillary/mandible dentures made with CADCAM (computer-aided design/computer-aided manufacturing) technology

    Device: Complete CADCAM dentures
    Arm 2-Standard Treatment Sequence for Digital Dentures in a Dental School Clinic (5 appointments): Appointment 1: Exam, diagnosis, & tray selection (begin impressions) Appointment 2: Definitive impressions and Maxillomandibula relations Appointment 3: Wax-trial arrangement Appointment 4: Insertion and instructions for care of definitive prosthesis Appointment 5: Post adjustment/s (Less post insertion adjustments are anticipated due to CADCAM milling of the denture base and less polymerization shrinkage
    Other Names:
  • complete digital dentures
  • Outcome Measures

    Primary Outcome Measures

    1. the overall comparison of functional assessment of digitally fabricated dentures to traditionally fabricated dentures [2 years]

      evaluate functional assessment of digitally fabricated dentures to traditionally fabricated dentures (FAD= Functional Assessment of Dentures)

    Secondary Outcome Measures

    1. comparison of functional assessment of digitally fabricated dentures to traditionally fabricated dentures [baseline = 4 weeks]

      evaluate functional assessment of digitally fabricated dentures to traditionally fabricated dentures (FAD= Functional Assessment of Dentures)

    2. comparison of functional assessment of digitally fabricated dentures to traditionally fabricated dentures [3 months]

      evaluate functional assessment of digitally fabricated dentures to traditionally fabricated dentures (FAD)

    3. comparison of functional assessment of digitally fabricated dentures to traditionally fabricated dentures [6 months]

      evaluate functional assessment of digitally fabricated dentures to traditionally fabricated dentures (FAD)

    4. comparison of functional assessment of digitally fabricated dentures to traditionally fabricated dentures [1 year]

      evaluate functional assessment of digitally fabricated dentures to traditionally fabricated dentures (FAD)

    5. comparison of patient satisfaction between digital dentures and traditional dentures [baseline = 4 weeks]

      patient satisfaction survey consisting of 12 items organized into 5 subscales (not at all satisfied, not very satisfied, reasonably satisfied, very satisfied, totally satisfied) and responses are based on a Likert scale

    6. comparison of patient satisfaction between digital dentures and traditional dentures [3 months]

      patient satisfaction survey consisting of 12 items organized into 5 subscales (not at all satisfied, not very satisfied, reasonably satisfied, very satisfied, totally satisfied) and responses are based on a Likert scale

    7. comparison of patient satisfaction between digital dentures and traditional dentures [6 months]

      patient satisfaction survey consisting of 12 items organized into 5 subscales (not at all satisfied, not very satisfied, reasonably satisfied, very satisfied, totally satisfied) and responses are based on a Likert scale

    8. comparison of patient satisfaction between digital dentures and traditional dentures [1 year]

      patient satisfaction survey consisting of 12 items organized into 5 subscales (not at all satisfied, not very satisfied, reasonably satisfied, very satisfied, totally satisfied) and responses are based on a Likert scale

    9. comparison of patient satisfaction between digital dentures and traditional dentures [2 year]

      patient satisfaction survey consisting of 12 items organized into 5 subscales (not at all satisfied, not very satisfied, reasonably satisfied, very satisfied, totally satisfied) and responses are based on a Likert scale

    10. bite force comparison between digital dentures and traditional dentures [baseline = 4 weeks]

      using gnathometer assessment, investigators will record the force (on a 0-10 scale) during dislodgement

    11. bite force comparison between digital dentures and traditional dentures [3 months]

      using gnathometer assessment, investigators will record the force (on a 0-10 scale) during dislodgement

    12. bite force comparison between digital dentures and traditional dentures [6 months]

      using gnathometer assessment, investigators will record the force (on a 0-10 scale) during dislodgement

    13. bite force comparison between digital dentures and traditional dentures [1 year]

      using gnathometer assessment, investigators will record the force (on a 0-10 scale) during dislodgement

    14. bite force comparison between digital dentures and traditional dentures [2 year]

      using gnathometer assessment, investigators will record the force (on a 0-10 scale) during dislodgement

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years to 99 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    Yes
    Inclusion Criteria:
    1. UNC School of Dentistry Student Clinic patients requiring maxillary and mandibular complete dentures

    2. Ages 18 to 99, inclusive

    3. Able to read, speak, and understand English

    4. Without natural tooth or implant supported overdentures

    5. Edentulous in both jaws for at least 6 months

    6. Any Prosthodontic Diagnostic Index (PDI) type with a preference given to Types 1-3

    Exclusion Criteria:
    1. Non-registered patient in UNC School of Dentistry student clinics

    2. Patient not able or unwilling to give consent

    3. Subject had extractions within last 6 months

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 University of North Carolina School of Dentistry Student Clinics Chapel Hill North Carolina United States 27599

    Sponsors and Collaborators

    • University of North Carolina, Chapel Hill
    • Global Dental Science, LLC

    Investigators

    • Principal Investigator: Robert F Wright, DDS FACP, Professor and Chair, Dept. of Prosthodontics UNC School of Dentistry

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    Responsible Party:
    University of North Carolina, Chapel Hill
    ClinicalTrials.gov Identifier:
    NCT02521935
    Other Study ID Numbers:
    • 14-1811
    First Posted:
    Aug 13, 2015
    Last Update Posted:
    Apr 27, 2017
    Last Verified:
    Apr 1, 2017
    Individual Participant Data (IPD) Sharing Statement:
    No
    Plan to Share IPD:
    No
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Apr 27, 2017