Complete Lower Dentures on 1 or 2 Implants

NCT02117856 · Status: ACTIVE_NOT_RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 86

Last updated 2019-06-19

No results posted yet for this study

Summary

This study is a randomized clinical trial to compare patient satisfaction and prosthetic outcomes with lower dentures retained by one or two implants. The investigators long-term objective is to establish evidence of the cost-effectiveness of a single implant intervention for improving tolerance to complete dentures. The investigators MAIN AIM will be to investigate patient satisfaction between and within groups with mandibular dentures retained by one or two implants over five years, and SECONDARILY to investigate the survival of implants, and the frequency of events to maintain the dentures and prosthetic attachments as clinically serviceable. Furthermore, multivariate analysis can assess the prediction of patient satisfaction with implant dentures based on various possible factors including age, health, demography and socioeconomic status, number of implants, and maintenance needs. Patient satisfaction will be measured by means of Visual Analogue Scales (VAS) including a measure of overall satisfaction and various specific aspects of satisfaction such as appearance, stability and comfort of the dentures.

The CENTRAL HYPOTHESIS is that mandibular complete dentures retained by single implants are at least as satisfying to patients over a five years period as those retained by two implants for the same period.

The SECONDARY HYPOTHESES are that:

i) there is no difference over five years between groups in the survival of original implants, or in the number of events for maintenance of the dentures or implant attachments; and ii) using each treatment group as it's own control, there is no change in patient satisfaction with lower dentures retained by either one or two implants during the five year loading period.

Conditions

  • Tooth-loss
  • Edentulous Mouth
  • Complete Denture
  • Complete Lower Denture

Interventions

PROCEDURE

1 implant placed surgically in the mandibular midline

Participants receive an implant in the mandibular midline using a surgical flap procedure with local anaesthesia.

PROCEDURE

2 implants placed surgically in the mandibular canine sites

Participants receive implants bilaterally in the site of the mandibular canines using a surgical flap procedure with local anaesthesia.

PROCEDURE

Soft reline (Coe Comfort) of the existing complete lower denture

Participants receive a soft reline of the existing complete lower denture approximately 10 days after placement of the implant(s).

DEVICE

2.25mm ball patrix placed on 1 healed implant

A 2.25mm ball patrix is screwed onto the 1 implant approximately six weeks after placement of the implant.

DEVICE

2.25mm ball patrices placed on 2 healed implants

2.25mm ball patrices are screwed onto the 2 implants approximately six weeks after placement of the implants.

PROCEDURE

Reline (Ivoclar acrylic-resin) with 1 retentive matrix in the lower denture

Participants have their complete lower denture relined with a laboratory-processed acrylic resin to incorporate 1 retentive matrix in the denture-base to retain on the implant.

PROCEDURE

Reline (Ivoclar acrylic-resin) with 2 retentive matrices in the lower denture

Participants have their complete lower denture relined with a laboratory-processed acrylic resin to incorporate 2 retentive matrices in the denture-base to retain on the implants

Sponsors & Collaborators

  • ITI International Team for Implantology, Switzerland

    collaborator OTHER
  • Canadian Institutes of Health Research (CIHR)

    collaborator OTHER_GOV
  • Straumann Canada Ltd.

    collaborator UNKNOWN
  • University of British Columbia

    lead OTHER

Principal Investigators

  • Stephen R. Bryant, DDS, PhD · University of British Columbia

  • Michael I. MacEntee, LDS, PhD · University of British Columbia

  • Joanne N. Walton, DDS · University of British Columbia

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2002-11-30
Primary Completion
2027-06-30
Completion
2027-06-30

Countries

  • Canada

Study Locations

More Related Trials

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02117856 on ClinicalTrials.gov