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Clinical pilot trial of diameter reduced implant retained overdenture prothesis in the edentulous mandible with 2 or 4 locatorlike attachments

Not Applicable
Completed
Conditions
K08.2
Atrophy of edentulous alveolar ridge
Registration Number
DRKS00005497
Lead Sponsor
Poliklinik für Zahnärztliche Prothetik
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
25
Inclusion Criteria

poitiv consent statement;
full age;
edentulous lower jaw;
adaquate bone in vertical and horizontal dimension;
informed about alternative treatment options; the advantages and disadvantages as well as corresponding costs;
decision against alternative treatment option;

Exclusion Criteria

A lack of consent, minority or limited legal capacity provide for the exclusion of patients from the study. There must be no change of location of the patient to be planned. Patients who suffer from bruxism (teeth grinding), pregnant and lactating women, and patients after Radatio in the jaw / face area, bisphosphonate therapy within the last ten years or bleeding diathesis are also excluded. Patients with inadequate bone, are also excluded from participation.

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Chancge of masticatory efficacy (chewing test) on lower jaw prothesis retained with/without llocatorlike attachments on interforaminal diameter reduced implants after 3, 6, and 9 months post operative<br>
Secondary Outcome Measures
NameTimeMethod
Test intervals: 3, 6, 9 and 12 months postoperative<br><br>Quality of Life before and after implant insertion with option A and B (questionaire OHIP)<br><br>Recording of functional change of stomatognathic by using EMG-Activity with option A and B<br><br>Patients' Expectation (Questionaire)<br><br>Prosthetic Complications (clinical examinsation)<br><br>Survivalrate of diameter reduced implants (clinical examinsation)<br><br>
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