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The Treatment of Implant-retained Mandibular Overdentures for Edentulous Patients

NCT02846805 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 53

Last updated 2020-04-21

No results posted yet for this study

Summary

The purpose of this study is to investigate to what extent IOs improve the functionality of edentulous patients and changes in quality of life and overall patient satisfaction following treatment with IOs.

Conditions

  • Edentulous

Interventions

PROCEDURE

implant-retained overdentures

subjects will receive two-implant-retained overdentures in the mandible,and they continue wearing their complete denture in the maxilla.

Sponsors & Collaborators

  • Chufan Ma

    lead OTHER

Principal Investigators

  • Chufan Ma · Air Force Military Medical University, China

Study Design

Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
40 Years
Max Age
75 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2016-05-31
Primary Completion
2018-07-31
Completion
2020-04-30

Countries

  • China

Study Locations

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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 NCT02846805 on ClinicalTrials.gov