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OpenTrials
Completed

NCT Number: NCT04301115

Unilateral Attachment Versus Tooth Implant Supported Bridge

Purpose: Evaluation of patients' satisfaction, biting force measurement and radiographic evaluation of abutment teeth of tooth implant supported bridge, unilateral attachment and conventional partial denture in mandibular distal extension cases.

Materials and methods: Twenty four patients were selected and divided into three equal groups, each of eight patients: patients of group I Patients received a fixed tooth implant supported bridge, patients of group II Patients received a removable unilateral attachment partial denture and group III Patients received a conventional removable partial denture.Evaluation included patient satisfaction and biting force measurement radiographic evaluation of terminal abutments.

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Key information

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Cairo University

Cairo, 11511, Egypt

About this study

Purpose: Evaluation of patients' satisfaction, biting force measurement and radiographic evaluation of abutment teeth of tooth implant supported bridge, unilateral attachment and conventional partial denture in mandibular distal extension cases.

Materials and methods: Twenty four patients were selected according to the following criteria: Patients with unilateral mandibular distal extension with last standing second premolar abutment, abutments showed sufficient occluso-gingival height and good periodontal condition. Patients were divided into three equal groups, each of eight patients: patients of group I Patients received a fixed tooth implant supported bridge, patients of group II Patients received a removable unilateral attachment partial denture and group III Patients received a conventional removable partial denture.Evaluation included patient satisfaction using "OHIP14" questionnaires and biting force measurement radiographic evaluation of terminal abutments.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Unilateral mandibular distal extension area
  • The abutments showed sufficient occluso-gingival height of its clinical crown
  • Adequate inter-arch space and no tempro-mandibular joint disorders.
  • No para-functional habits,
  • Full opposing arch or restored with acceptable fixed restoration
  • Minimal bone height11 mm at the lower second molar area.

Exclusion criteria

*Insufficent bone height in posterior area of mandible

Treatment and study plan

attachment

Other

unilateral attachment from rehine 83

bridge

Other

tooth implant supported bridge

Conventional

Other

conventional metalic partial denture

Other names: partial denture

Primary outcomes

  1. patient satisfaction

    Time frame: 1 month

    questionnaires

Secondary outcomes

  1. biting force

    Time frame: 1 month

    measuring the biting force of the patients by sensor

  2. radiographic evaluation

    Time frame: 1 month

    evaluation of alveolar bone loss

Sponsors and collaborators

Lead sponsor

Cairo University

Other

Registry information

Official study title

Attachment-retained Unilateral Partial Denture Versus Tooth Implant Supported Prosthesis in Mandibular Distal Extension Cases

Important dates

Study start
2018
Primary completion
2019
Study completion
2019
First posted
Mar 10, 2020
Registry last updated
Mar 10, 2020

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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