Immediate load of implant retained overdenture prothesis on the edentulous mandible

Not Applicable

• Conditions: K08.2; Atrophy of edentulous alveolar ridge

• Registration Number: DRKS00004245
• Lead Sponsor: Poliklinik für Zahnärztliche Prothetik

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2012-10-19
• Study Completion: 2014-11-30
• Last Update Posted: 19 August 2024

Recruitment & Eligibility

• Status: Complete
• Sex: All
• Target Recruitment: 46

Inclusion Criteria

positiv consent statement;
full age;
edentulous lower jaw;
adequate bone in vertical and horizonal dimension;
informed about alternative treadment options, there advantes and disadvantages as well as correspondings 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

Name	Time	Method
Recalls after 3, 6, 12, and 24 month. the examination in clinically cumulative survivalrate of implants

Secondary Outcome Measures

Name	Time	Method
qualitiy of life, mastication <br>masticatory power<br>prosthetic complications<br><br>Recalls after 3, 6, 12, and 24 month. the examination in clinically