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Accuracy of Dynamic Navigation System on Zygomatic Implant Placement

Not Applicable
Recruiting
Conditions
Surgery, Computer-Assisted
Dental Implants
Interventions
Device: Freehand zygomatic implant placement
Registration Number
NCT06155799
Lead Sponsor
University of Barcelona
Brief Summary

This study consists in a randomized controlled trial which objective is to assess the accuracy of a dynamic navigation system in zygomatic implant placement in partially or total edentulous patients in the upper jaw compared with the conventional freehand method.

Detailed Description

The present study is a prospective randomized clinical trial.

Each patient enrolled in this trial will be randomly allocated to on group (Navigation group (test group) or Freehand group (control group)). Preoperative virtual planification of zygomatic an conventional implants on a prerequired cone beam computed tomography (CBCT) with radiographic markers (tooth if possible or micro implants if not possible) will be performed for each patient.

The patient will be randomly allocated in one group just before the surgery, and the surgical procedure will be performed according the surgery protocol of each group. Then, after the surgical procedure a PROMs questionnaire will be asked to the patients.

Finally a postoperative CBCT will be performed and overlapped with the preoperative CBCT with the implants planification and implant position deviations between the planned and final position will be measured.

The study devices are European Conformity (CE) marked products and used within their intended use.

Recruitment & Eligibility

Status
RECRUITING
Sex
All
Target Recruitment
8
Inclusion Criteria
  • Partial or total edentulous maxilla
  • Large bone atrophy that avoids possible conventional implant placement
  • Over 18 years old patients
Exclusion Criteria
  • Patients with facial bone disease that contraindicates conventional or zygomatic implants placement.
  • Systemic or local conditions that contraindicates oral surgery.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Freehand groupFreehand zygomatic implant placementZygomatic implant placement by Freehand, without any guidance.
Navigation groupFreehand zygomatic implant placementZygomatic implant placement by dynamic computer assisted surgery system.
Primary Outcome Measures
NameTimeMethod
Platform 3D deviation1 month

Global deviation at the platform of the zygomatic implant between the virtual planned position and the final position of the dental implant measured in the 3 axes of the space (3D deviation). Measured in millimeters (mm).

Apex 3D deviation1 month

Global deviation at the apex of the dental implant between the virtual planned position and the final position of the dental implant measured in the 3 axes of the space (3D deviation). Measured in millimeters (mm).

Angular deviation1 month

Angular deviation between the virtual planed position of the implant and the final implant position. Measured in degrees

Secondary Outcome Measures
NameTimeMethod
Patient-reported outcome measures questionnaireOne week post operative

Patients perception of therapy functional well-being and health status during the dental implant treatment with a navigation system. The scale goes from 0 to 4, where higher scores mean worse outcome.

Complications6 months

Number of intra and postoperative complications and what kind of complication it was.

Time of surgery24 hours

Two times of surgery were recorded: time of drilling, from the first drilling of the first zygomatic implant to the last zygomatic implant placement; and time of complete surgery procedure, from first incision to suture.

Trial Locations

Locations (1)

Hospital Odontológic de Barcelona

🇪🇸

L'Hospitalet De Llobregat, Barcelona, Spain

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