Survival of 3D-planned and template-based implants inserted depending on the pre-implant hard and soft tissue management - a randomized controlled clinical trial

Not Applicable

Conditions: K08.1
Loss of teeth due to accident, extraction or local periodontal disease

Registration Number: DRKS00005978

Lead Sponsor: niversitätsklinikum Ulm/Studienleiter: Prof. Dr. Ralph G. Luthardt, Klinik für Zahnärztliche Prothetik

Brief Summary: Not available

Detailed Description: Not available

Recruitment & Eligibility

Status: Complete

Sex: All

Target Recruitment: 60

Inclusion Criteria

Patients where the removal of a tooth in the upper jaw is necessary and where a supply of a implant is planned.
All patients come from the study before.

Exclusion Criteria

• Persons under 18 or not legally competent persons
• Detectable primary additional for augmentation need
• insertion of the implant with a Drilling template not possible (no sufficient mouth opening).
• Heavy smokers (more than 10 cig. / Day)
• use of bisphosphonates
• Pregnant
• Alcohol or drug addicts
• Patients with an infectious disease such as hepatitis or HIV or AIDS
• Patients with severe diabetes m.

Study & Design

Study Type: interventional

Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Primary target of the analysis is the loss of the implant differentiated in an observation period of 5 years after insertion by the two groups with / without pre-implant hard and soft tissue management. In addition to target size, the accuracy of 3D implant position compared to 3D planning.

Secondary Outcome Measures

Name	Time	Method
Other side targets biological and technical complications are subdivided into the two groups with / without pre-implant hard and soft tissue studied. In addition, patient satisfaction (VAS), the Pink Aesthetic score after Fürhauser et al are. 2005, the primary stability of the implant (Osstell ISQ) and the subsequent stability of the implant-served (periotest) and the efficiency of the method comparatively evaluated.<br>Acquisition of data: baseline at the completion of prosthetic services, 1/2 year later, 1, 2, 3 and 5 years later