Clinical Results of Implant-retained Mandibular Overdentures in Edentulous Patients

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Total Enrollment

54 participants

Study Classification

OBSERVATIONAL

Study Start Date

2016-02-29

Study Completion Date

2017-08-31

Brief Summary

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The purpose of this study is to evaluate the clinical results of implant-retained mandibular overdentures in edentulous patients.

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Detailed Description

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The survival of implants,condition of the peri-implant soft tissue were evaluated. And patients' perceptions regarding the outcome were assessed on visual analog scales (VAS), oral health impact profile-14 (OHIP) and semantic differential scale questionnaires.

Conditions

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Edentulous

Study Design

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Observational Model Type

COHORT

Study Time Perspective

RETROSPECTIVE

Study Groups

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implant retained-overdentures with the attachment of bar

patients treated with implant-retained overdentures,and the attachment is bar

implant-retained overdentures

Intervention Type DEVICE

patients treated with an implant-retained overdenture in the mandible

implant retained-overdentures with the attachment of magnet

patients treated with implant-retained overdentures,and the attachment is magnet

implant-retained overdentures

Intervention Type DEVICE

patients treated with an implant-retained overdenture in the mandible

Interventions

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implant-retained overdentures

patients treated with an implant-retained overdenture in the mandible

Intervention Type DEVICE

Eligibility Criteria

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Inclusion Criteria

1. Patients treated with implant retained overdentures
2. With the ability to read and sign the informed consent document

Exclusion Criteria

1. Jaw radiotherapy treatment before and after implanting
2. Patients who suffered with mental and psychological disease will influence their oral health normal maintenance
3. Can not read and sign the informed consent document

Minimum Eligible Age

45 Years

Maximum Eligible Age

83 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes