Fully Versus Partially Guided Implants Placement: Measurement of Accuracy of Implant Position and… (NCT07174791) | Clinical Trial Compass
Active — Not RecruitingNot Applicable
Fully Versus Partially Guided Implants Placement: Measurement of Accuracy of Implant Position and Passivity of Superstructures.
Egypt16 participantsStarted 2025-01-15
Plain-language summary
compare fully versus partially guided all on four implants placement immediately loaded by maxillary and mandibular screw retained overdentures: A radiographic and photogrammetric measurement of accuracy of implant position and passivity of superstructures.
The measurements will be done as follows:
1. Photogrammetric scan immediately after implant instalments to measure 3D accuracy of implant position and Passivity of super structure
2. Cone beam X ray to measure the implant marginal bone height changes.
3. Implant marginal soft tissue evaluations including pocket probing depth, plaque and gingival indices. Evaluation will be done immediately, one and two years after loading.
Who can participate
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:
* Completely healed residual alveolar ridges
* Angle's class I maxillo-mandibular relationship.
* Sufficient mandibular and maxillary restorative spaces, at least 15mm evaluated by recording a tentative jaw relation.
* Adequate bone height in the premaxilla area, and the anterior mandibular area. - This will be evaluated radiographically
Exclusion Criteria:
* Systemic disorders affecting bone (such as uncontrolled diabetes mellitus and osteoporosis).
* Local or general contraindication for surgical procedures.
* History of chemotherapy or radiation therapy to the head and neck area.
* Poor neuromuscular co-ordination.
* TMJ dysfunction and parafunctional habits
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.