The influence of the type of drilling in the success of dental implants: Randomized clinical trial

Not Applicable

Recruiting

• Conditions: D25.339.312; Dental implants.; K09.1; extraction or localized periodontal disease; oss of teeth due to accident

• Registration Number: RBR-6vs56t
• Lead Sponsor: niversidade Federal de Pelotas

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2020-01-20
• Last Update Posted: 29 May 2023

Recruitment & Eligibility

• Status: Recruiting
• Sex: Not specified
• Target Recruitment: Not specified

Inclusion Criteria

This project will be submitted for approval by the Research Ethics Committee of the UFPel School of Dentistry, prior to its completion.
To be included in the sample, patients will need to have the following characteristics:
Present edentulism with an indication of dental implant installation and subsequent dental prosthesis or indication of extraction of a dental element by crack/fracture or root perforation with an indication for immediate dental implant installation and subsequent dental prosthesis; Have a good general state of health that allows dental implant surgery; Have time and time available to attend dental appointments at institutions.

Exclusion Criteria

Patients with any of the following characteristics may not be part of the sample: Patient with any systemic disease that prevents surgery for dental implant installation; Patients with a history of chemo/radiotherapy in the last 10 years or who use systemic medications that may interfere with bone repair (eg, bisphosphonates); Patients who do not have time available for care in educational institutions.

Study & Design

• Study Type: Intervention
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Primary outcomes<br>The primary outcome to be evaluated will be the survival of implants, which refers to the implant being in its position of installation, at the moment of consultation, regardless of the condition of the other components / tissues related to it (bone, soft tissue, prosthetic abutment). screw, prosthetic crown, etc.) (Zarb and Albrektsson, 1998).

Secondary Outcome Measures

Name	Time	Method
Secondary outcomes relate to the success of the implant, and the fact that all surrounding tissues have a satisfactory condition (Zarb and Albrektsson, 1998). For this study the outcomes evaluated will be probing depth, gingival bleeding, gingival retraction, bone loss around the implant, volumetric change and peri-implant soft tissue condition, and patient satisfaction.