Precision of Three Different Scanbodies Used for Direct Digitalization Technique (NCT05790148) | Clinical Trial Compass
CompletedNot Applicable
Precision of Three Different Scanbodies Used for Direct Digitalization Technique
Turkey (Türkiye)25 participantsStarted 2020-08-11
Plain-language summary
The goal of this clinical trials to evaluate precision of different scanbodies in same participant group. The main guestion it aim to answer is:
1\. Are the precision of the three different scanbodies used in direct digitalization the same for the produce of implant-supported prostheses?
Participants are healty and have short edentulous span in posterior region that will receive implant-supported prostheses.
Who can participate
Age range
18 Years
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria:
* Be willing to voluntarily participate in the study after reading the informed consent form.
* Adult patient over 18 years of age who has completed growth and development
* Partial edentulism in the functional region for a two-implant-supported restoration with two or three occlusal members
* Having a fixed dentition in the opposing arch
* The occlusal relationship between the jaws does not require vertical and horizontal prosthetic treatment.
* Having bone-level implants placed with "straightforward" surgery according to the SAC classification system \[248\] and without advanced surgical technique
Exclusion Criteria:
* Not voluntarily agreeing to participate in the study after reading the informed consent form
* Having one or more of the conditions for which implant treatment is strictly contraindicated (patients who have received radiation therapy, bone cancer, metabolic disorders)
* Having systemic (steroid therapy, uncontrolled diabetes, immunological disorders, pregnancy) risk factors for implant treatment
* Having local (periodontal discomfort, bruxism, poor oral hygiene) risk factors for implant treatment
Questions worth asking your doctor
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
Questions for the trial coordinator
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.