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Cost-effectiveness of the Single-implant Mandibular Overdenture Versus Mandibular Conventional Denture

Primary Purpose

Mouth, Edentulous, Complete Edentulism

Status
Completed
Phase
Not Applicable
Locations
Brazil
Study Type
Interventional
Intervention
Mandibular overdenture
Mandibular complete denture
Sponsored by
Universidade Federal de Goias
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Mouth, Edentulous focused on measuring overdenture, edentulism, dental implant, cost-effectiveness, economic analysis, effectiveness

Eligibility Criteria

undefined - undefined (Child, Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • To present favorable general health and the need to be rehabilitated with a new set of complete dentures
  • To agree to be randomly assigned to one of the two study groups
  • To be able to comprehend and answer the data collection instruments.

Exclusion Criteria:

  • Presence of general health conditions that may contraindicate implant surgery (such as uncontrolled type II diabetes mellitus or uncontrolled cardiovascular conditions)
  • Insufficient height and volume in the midline region to receive an implant of at least 3.75mm x 9.0mm
  • Presence of evident signs of cognitive impairment and/or oral conditions requiring additional treatments, such as oral lesions and temporomandibular disorders
  • Inability to attend to the scheduled appointments and follow-up visits

Sites / Locations

  • School of Dentistry, Federal University of Goias

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Single-implant mandibular overdenture

Mandibular complete denture

Arm Description

Participants allocated to this group will have a dental implant placed in the mandibular midline followed by the immediately insertion of a ball attachment and the incorporation of a retention matrix to the mandibular denture.

Participants allocated to this group will not receive any additional treatment besides the new set of conventional complete dentures. When needed, retreatment or any adjustment/repair in the dentures will be performed accordingly. Participants will receive regular maintenance for their dentures, including adjustments for the elimination of sore areas, denture relining and repair of fractures, when needed, until the end of the follow-up period.

Outcomes

Primary Outcome Measures

Oral health-related quality of life (OHRQoL)
The cross-culturally adapted Brazilian version of the Oral Health Impact Profile for edentulous subjects (OHIP-EDENT) will be used. It contains 19 items divided in four different subscale domains: (I) masticatory discomfort and disability (four items), (II) psychological discomfort and disability (five items), (III) social disability (five items), and (IV) oral pain and discomfort (five items). The items are answerable by a 3-point Likert scale and responses will be summed to result an overall score. Higher scores represent worse OHRQoL.

Secondary Outcome Measures

Satisfaction with the dentures
Participants will report how satisfied they are on a 0-100 scale by choosing a multiple of 10. Zero will be considered the least satisfied possible and "100" the most satisfied possible.

Full Information

First Posted
March 5, 2018
Last Updated
March 9, 2018
Sponsor
Universidade Federal de Goias
Collaborators
Conselho Nacional de Desenvolvimento Científico e Tecnológico
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1. Study Identification

Unique Protocol Identification Number
NCT03463174
Brief Title
Cost-effectiveness of the Single-implant Mandibular Overdenture Versus Mandibular Conventional Denture
Official Title
A Randomized Controlled Clinical Trial Alongside a Cost-effectiveness Analysis of the Mandibular Conventional Complete Denture Versus Single-implant Mandibular Overdenture
Study Type
Interventional

2. Study Status

Record Verification Date
March 2018
Overall Recruitment Status
Completed
Study Start Date
March 10, 2015 (Actual)
Primary Completion Date
September 20, 2017 (Actual)
Study Completion Date
October 31, 2017 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Universidade Federal de Goias
Collaborators
Conselho Nacional de Desenvolvimento Científico e Tecnológico

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
This is a randomized clinical trial designed to assess the 1-year effectiveness of two treatment modalities for the mandibular edentulists: conventional complete dentures and single-implant mandibular overdenture.
Detailed Description
This randomized clinical trial alongside a cost-effectiveness analysis will include edentulous individuals who meet eligibility criteria. New maxillary and mandibular dentures will be fabricated for all participants following a standardized protocol. Then, participants will be randomized into one of the treatment groups: conventional complete denture group or single-implant mandibular overdenture group. Each participant allocated to the overdenture group will then receive an implant (Titamax TI cortical - Neodent, Brazil) in the mandibular midline followed by the immediate connection of an O-Ring/ball attachment with intra-oral incorporation of the retention system in the mandibular denture. Direct costs related to therapies in both groups will be identified, measured and valuated for one year after treatment and patient-reported outcomes will be assessed. Incremental cost-effectiveness ratios will be estimated and graphically presented on cost-effectiveness planes. A Markov decision tree will be constructed to set out the consequences of the competing alternatives. Sensitivity analysis on the most important assumptions will be performed in order to assess the robustness of the model.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Mouth, Edentulous, Complete Edentulism
Keywords
overdenture, edentulism, dental implant, cost-effectiveness, economic analysis, effectiveness

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
80 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Single-implant mandibular overdenture
Arm Type
Experimental
Arm Description
Participants allocated to this group will have a dental implant placed in the mandibular midline followed by the immediately insertion of a ball attachment and the incorporation of a retention matrix to the mandibular denture.
Arm Title
Mandibular complete denture
Arm Type
Active Comparator
Arm Description
Participants allocated to this group will not receive any additional treatment besides the new set of conventional complete dentures. When needed, retreatment or any adjustment/repair in the dentures will be performed accordingly. Participants will receive regular maintenance for their dentures, including adjustments for the elimination of sore areas, denture relining and repair of fractures, when needed, until the end of the follow-up period.
Intervention Type
Procedure
Intervention Name(s)
Mandibular overdenture
Other Intervention Name(s)
Dental Implant (Straumann StandardPlus SLActive® RN implant)
Intervention Description
Placement of an implant in the mandibular midline.
Intervention Type
Other
Intervention Name(s)
Mandibular complete denture
Other Intervention Name(s)
Complete denture
Intervention Description
No intervention.
Primary Outcome Measure Information:
Title
Oral health-related quality of life (OHRQoL)
Description
The cross-culturally adapted Brazilian version of the Oral Health Impact Profile for edentulous subjects (OHIP-EDENT) will be used. It contains 19 items divided in four different subscale domains: (I) masticatory discomfort and disability (four items), (II) psychological discomfort and disability (five items), (III) social disability (five items), and (IV) oral pain and discomfort (five items). The items are answerable by a 3-point Likert scale and responses will be summed to result an overall score. Higher scores represent worse OHRQoL.
Time Frame
From baseline to 12 months after the intervention
Secondary Outcome Measure Information:
Title
Satisfaction with the dentures
Description
Participants will report how satisfied they are on a 0-100 scale by choosing a multiple of 10. Zero will be considered the least satisfied possible and "100" the most satisfied possible.
Time Frame
From baseline to 12 months after the intervention
Other Pre-specified Outcome Measures:
Title
Costs
Description
All the direct dental costs related to the clinical and laboratory phases of both treatment groups will be listed, measured and valued.
Time Frame
From denture's fabrication to 12 months after the intervention

10. Eligibility

Sex
All
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: To present favorable general health and the need to be rehabilitated with a new set of complete dentures To agree to be randomly assigned to one of the two study groups To be able to comprehend and answer the data collection instruments. Exclusion Criteria: Presence of general health conditions that may contraindicate implant surgery (such as uncontrolled type II diabetes mellitus or uncontrolled cardiovascular conditions) Insufficient height and volume in the midline region to receive an implant of at least 3.75mm x 9.0mm Presence of evident signs of cognitive impairment and/or oral conditions requiring additional treatments, such as oral lesions and temporomandibular disorders Inability to attend to the scheduled appointments and follow-up visits
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Claudio R Leles, DDS, PhD
Organizational Affiliation
Universidade Federal de Goias
Official's Role
Study Director
Facility Information:
Facility Name
School of Dentistry, Federal University of Goias
City
Goiânia
State/Province
Goias
ZIP/Postal Code
74605-220
Country
Brazil

12. IPD Sharing Statement

Plan to Share IPD
Undecided
Citations:
PubMed Identifier
30006117
Citation
Nogueira TE, Aguiar FMO, Esfandiari S, Leles CR. Effectiveness of immediately loaded single-implant mandibular overdentures versus mandibular complete dentures: A 1-year follow-up of a randomized clinical trial. J Dent. 2018 Oct;77:43-50. doi: 10.1016/j.jdent.2018.07.006. Epub 2018 Jul 10.
Results Reference
derived

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Cost-effectiveness of the Single-implant Mandibular Overdenture Versus Mandibular Conventional Denture

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