Actively Recruiting
Precision, Patient Satisfaction and Timing of Complete-arch Digital Implant Impression Using Conventional Impression, Intraoral Scanner, and Photogrammetry Techniques
Led by Centre Hospitalier Universitaire de Liege · Updated on 2024-08-26
20
Participants Needed
1
Research Sites
10 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Researchers are evaluating the precision of different implant-supported impression techniques in patients without teeth (edentulous) who have 4 to 8 osseointegrated implants in the upper or lower jaw. This clinical trial compares conventional impressions, intraoral scanners, and photogrammetry to determine which method provides the most accurate complete-arch impression. Additionally, the study aims to assess patient satisfaction with these new impression methods. Each participant will undergo six impressions in total: two with an intraoral scanner, two with photogrammetry, and two conventional plaster impressions using an open tray technique. The procedures are performed twice per method on the same day. After each type of impression, patients will complete a satisfaction questionnaire using a Visual Analogue Scale (VAS) to rate comfort, anxiety, taste, nausea, pain, and treatment length. The time taken for each impression is also recorded. Participants will attend a single appointment lasting about one hour during which all impressions and questionnaires are completed. Researchers will analyze the repeatability and precision of each impression technique and collect patient-reported outcome measures. The primary outcome is the precision of the complete-arch impression, and secondary outcomes include patient satisfaction ratings. This study includes safety monitoring and careful data collection to understand the patient experience with these digital and conventional impression methods.
CONDITIONS
Brief Title
Comparison of Conventional Impressions, Intraoral Scanners and Digital Photogrammetry for Full-arch Implant Prosthesis.
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Edentulous upper or lower jaw with 4 to 8 osseointegrated implants
- Implants must be NobelBiocare system with transgingival abutments tightened to 35N/cm
- Adults aged 18 years and older
You will not qualify if you...
- Patients with implants that are not osseointegrated
- Patients using implant systems other than NobelBiocare
- Patients who do not have complete tooth loss in the jaw being studied (incomplete edentulism)
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - 1 hour
Participants undergo six implant impressions in one appointment, including two conventional impressions, two intraoral scanner impressions, and two photogrammetry impressions. After each type of impression, participants complete a satisfaction questionnaire.
1 visit (in-person)
Trial Site Locations
Total: 1 location
1
Institut de Dentisterie
Liège, Liege, Belgium, 4000
Actively Recruiting
Research Team
N
Nathalie Robert, DDS
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
SCREENING
Number of Arms
1
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