Comparing Dynamic Navigation to Static Navigation in the Implant Placement
RCT
Accuracy Assessment of Dynamic Vs. Static Navigation Implant Placement Protocols (Randomized Controlled Trial)
1 other identifier
interventional
20
1 country
1
Brief Summary
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
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for phase_4
Started Oct 2022
Typical duration for phase_4
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
Study Start
First participant enrolled
October 1, 2022
CompletedFirst Submitted
Initial submission to the registry
November 22, 2025
CompletedFirst Posted
Study publicly available on registry
December 18, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
January 1, 2026
CompletedStudy Completion
Last participant's last visit for all outcomes
January 1, 2026
CompletedDecember 18, 2025
November 1, 2025
3.3 years
November 22, 2025
December 5, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Deviation
Deviation in Apical position, platform position and angular deviation
Baseline, Day 0
Secondary Outcomes (2)
Patient Satisfaction Questionnaire
1 week
Time
Perioperative/ Periprocedural
Study Arms (2)
sCAIS
ACTIVE COMPARATORdCAIS
EXPERIMENTALInterventions
Dynamic navigation system called MiniNavident
Eligibility Criteria
You may qualify if:
- 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.
You may not qualify if:
- 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
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Ain Shams University, Faculty of Dentistry
Cairo, Egypt
Study Design
- Study Type
- interventional
- Phase
- phase 4
- Allocation
- RANDOMIZED
- Masking
- SINGLE
- Who Masked
- OUTCOMES ASSESSOR
- Purpose
- OTHER
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Assistant Lecturer
Study Record Dates
First Submitted
November 22, 2025
First Posted
December 18, 2025
Study Start
October 1, 2022
Primary Completion
January 1, 2026
Study Completion
January 1, 2026
Last Updated
December 18, 2025
Record last verified: 2025-11
Data Sharing
- IPD Sharing
- Will share
- Shared Documents
- STUDY PROTOCOL
All IPD will be shared