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Recruiting NCT07291336

Comparing Dynamic Navigation to Static Navigation in the Implant Placement

Phase IV Interventional Healthy Adults Dental Implant Accuracy

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Dynamic navigation system, Static Implant guide.
Who it may be relevant to
Registry conditions: Healthy Adults, Dental Implant, Accuracy. Basic parameters: 22 years — 60 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Egypt
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

Accuracy Assessment of Dynamic Vs. Static Navigation Implant Placement Protocols (Randomized Controlled Trial)

Overview

Implant placement is preplanned by taking xrays and impressions for the mouth one group a guide is fabricated and used to guide the implant drilling all through to the implant placement the other group, no guide is fabricated, but the implant is placed by dynamic navigation through looking in a screen and checking where the implant is fully placed

Interventions

  • Device Dynamic navigation system
    Dynamic navigation system called MiniNavident
  • Device Static Implant guide
    Tooth supported guide is prefabricated before the surgery

Primary outcome measures

  • Deviation [Time frame: Baseline, Day 0]
Secondary outcome measures (2)
  • Patient Satisfaction Questionnaire [Time frame: 1 week]
  • Time [Time frame: Perioperative/ Periprocedural]

Eligibility criteria

Inclusion criteria

  • Healthy patients at least 22 years old.
  • At least one missing tooth to be restored using an implant in the upper jaw from the maxillary right 2nd premolar to the maxillary left 2nd premolar.
  • At least six residual teeth in the affected jaw (5).
  • Minimum of 5 mm available bone.

Exclusion criteria

  • Medical condition or medication that would impair bone healing.
  • Poor oral hygiene
  • Inadequate bone width or height that may need bone augmentation. 5
  • Alcohol users.
  • Smoking more than 10 cigarettes per day.
  • History of head and neck radiotherapy.
  • Pregnant females.
  • Uncontrolled hypertensive or diabetic patient.
  • Vulnerable group; prisoners, pregnant women, orphans…etc

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Single blind
Primary purpose
Other

Study locations

Egypt · 1 center
  • Ain Shams University, Faculty of Dentistry — Cairo

Identifiers

NCT: NCT07291336 · 1113

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗