Implants Immediately Installed in Esthetic Area With Computer-guided Surgery

Not Applicable

Active, not recruiting

• Conditions: Dental Implants

• Registration Number: NCT03986164
• Lead Sponsor: University of Campinas, Brazil

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2019-6-11
• Last Update Posted: 2 September 2024

Recruitment & Eligibility

• Status: Active, not recruiting
• Sex: All
• Target Recruitment: Not specified

Inclusion Criteria

Inclusion Criteria:<br><br> - Patients with sufficient bone volume availability apically and palatally that allows<br> the correct positioning of the implants (Kan et al, 2011);<br><br> - Implants with primary stability of 20-45 N (Gallucci et al, 2014);<br><br> - Patients with teeth to be extracted in the Class I, II or III corono-radicular<br> position, according to Kan et al. (2011);<br><br> - Patients with distance from the bone crest to the point of contact in adjacent teeth<br> less than or equal to 6.5mm (Buser et al 2017).<br><br>Exclusion Criteria:<br><br> - Presence of diabetes, blood disorders and systemic diseases that prevent the<br> surgical procedure;<br><br> - History of radiotherapy in the head or neck region;<br><br> - History of treatment with bisphosphonates;<br><br> - Pregnant or lactating women;<br><br> - Patients with teeth to be extracted in the Class V corono-radicular position,<br> according to Kan et al. (2011);<br><br> - Gingival recession in the teeth indicated for exodontia (Kan et al, 2001);<br><br> - Acute infection at the implant site (Morton et al, 2014);<br><br> - Unavailability to attend the FOP / UNICAMP on the pre-determined days.

Exclusion Criteria

Not provided

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Position of the implant

Secondary Outcome Measures

Name	Time	Method
Relative gingival margin position;Peri-implant probing depth;Relative clinical attachment level