Evaluation of Implant Placement by digital method

Not Applicable

Recruiting

• Conditions: K08.40; Partial loss of teeth, unspecified cause.; Partial loss of teeth, unspecified cause

• Registration Number: IRCT20211208053334N1
• Lead Sponsor: Tehran University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 29 August 2022

Recruitment & Eligibility

• Status: Recruiting
• Sex: All
• Target Recruitment: 14

Inclusion Criteria

at least two months after tooth extraction
acceptable occlusion

Exclusion Criteria

presence of a systemic disease
smoking
contraindication for surgical procedures
presence of parafunctional habits
presence of TMJ complications
need for graft or sinus lift surgery

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
The difference in implant angulation of designed and actual implants. Timepoint: immediately after surgery. Method of measurement: post-surgical CBCT.;The difference in apex location of designed and actual implants. Timepoint: immediately after surgery. Method of measurement: post-surgical CBCT.

Secondary Outcome Measures

Name	Time	Method
The difference in placement angle of designed and actual crowns. Timepoint: two weeks after surgery and placement of the temporary restoration. Method of measurement: post-operative intraoral scanning.;The difference in crown depth of designed and actual crowns. Timepoint: two weeks after surgery and placement of the temporary restoration. Method of measurement: post-operative intraoral scanning.;Early Implant Failure. Timepoint: up to three months after surgery. Method of measurement: clinical and radiographic examination.;Bleeding on Probing. Timepoint: 3 months after surgery. Method of measurement: periodontal probing.;Peri-implant probing depth. Timepoint: 3 months after surgery. Method of measurement: periodontal probing.