Status:
COMPLETED
Navigated Photogrammetry Compared to Standard Stereophotogrammetry
Lead Sponsor:
X-Nav Technologies, LLC
Conditions:
Doctor Efficiency
Dental Prosthesis Fit
Eligibility:
All Genders
21+ years
Brief Summary
The purpose of this study is to compare the clinical outcome of Navigated Photogrammetry to standard stereophotogrammetry techniques in digital dentistry for the following two parameters: * The amoun...
Detailed Description
Prior to implant surgery, a patient treatment plan is developed using a cone-beam computed tomography (CBCT), Intra Oral Scan (IOS), or digitized analog records. These records are loaded into a comput...
Eligibility Criteria
Inclusion
- Adult patients requiring dental implant reconstruction who would undergo implant surgery with or without participation in the study.
- The patient must need at least four implants placed in one or both jaws of the maxilla or mandible.
- All patients must undergo informed consent and willingly read, understand, and accept the risks and benefits associated with the study.
- Willingness to participate for the duration of the study of at least six months follow-up
- Is healthy enough to undergo implant surgery. i.e. patient is classified by the American Society of Anesthesiology Scale (ASA) physical status classification status as ASA 1, 2 or 3.
- Ample bone to fully accommodate the implants without impinging on vital structures.
Exclusion
- Patients who are not candidates for implant placement.
- Children and adolescents under 21 years of age.
- Refusal to sign informed consent.
- Less than four implants need to be restored.
- Severely immunocompromised patients
- Patients undergoing chemotherapy
- Pregnant females.
- Classified by the ASA physical status classification status as ASA \> 3,
- Patient at high risk for medication induced osteonecrosis of the jaw or any other medical condition that would preclude implant placement,
- Any systemic or local disease or condition that would compromise post healing and /or osseointegration.
- Need for systemic corticosteroids or any other medication that would compromise postoperative healing and / or osseointegration.
- Current alcohol or drug abuse.
- Inability or willingness to return for follow-up visits for the period of the study.
Key Trial Info
Start Date :
July 20 2024
Trial Type :
OBSERVATIONAL
Allocation :
ACTUAL
End Date :
May 23 2025
Estimated Enrollment :
4 Patients enrolled
Trial Details
Trial ID
NCT06506747
Start Date
July 20 2024
End Date
May 23 2025
Last Update
June 4 2025
Active Locations (1)
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1
Capital Center For Oral and Maxillofacial Surgery and For Cosmetic Surgery
Washington D.C., District of Columbia, United States, 20037