MGUIDE MORE Dental Implant Planning System- Clinical Accuracy Study

Status

Completed

Phases

Study type

Interventional

Source

ClinicalTrials.gov

Registry ID

NCT02217774

Enrollment

Registered

2014-08-15

Start date

2014-11-30

Completion date

2015-08-23

Last updated

2017-09-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Focus of Study: Computer-Aided Design/Instrumentation

Keywords

Computer-Aided Design/instrumentation, Cone-Beam Computed Tomography, Dental Implant, MGuide

Brief summary

The aim of the present study is to assess the accuracy of MGUIDE MORE System (MGS), consisting of MGUIDE MORE software, MGUIDE MORE surgical kit and MGUIDE MORE template by evaluating the difference between planned and actual implant positions on pre- and post-operative CBCTs.

Detailed description

Patients, attending the Department of Periodontology at the Rambam School of Graduate Dentistry, who are scheduled for implant therapy, will be screened for the study. Patients will be referred for CBCT of the upper/lower jaw as appropriate. DICOM data of the patient will be uploaded to MGUIDE software and used for diagnosis and treatment planning of the case. Surgery will be performed using MGUIDE MORE template and MGUIDE MORE surgical kit. Pre-operative and post-operative CBCT will be used for assessment of the difference between planned and actual implant positions.

Interventions

DEVICEMGUIDE MORE

MGUIDE MORE System (MGS), consisting of MGUIDE MORE software, MGUIDE MORE surgical kit and MGUIDE MORE template, will be used for planning, drilling and inserting dental implants.

Study design

Allocation

Intervention model

SINGLE_GROUP

Primary purpose

DIAGNOSTIC

Masking

NONE

Eligibility

Sex/Gender

ALL

Age

18 Years to No maximum

Healthy volunteers

Yes

Inclusion criteria

* Signed and dated inform consent form. * Age between 18+. * Patient expresses his wish to restore the missing tooth/teeth with dental implants. * Patient is examined and found suitable for implant therapy * Patient can open mouth sufficiently for preparation and placement of dental implants using the contra-angle handpiece and drills. * CBCT is required for proper diagnosis and treatment planning.

Exclusion criteria

Design outcomes

Primary

Measure	Time frame	Description
Deviation from planning	0-14 days after implant placement	To assess shoulder and apex deviations in milimeters between planned and actual implant position and to assess angular deviation in degrees, of actual implant position vs. planned implant position

Countries

Israel

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026