CompletedNot Applicable

Evaluation of Digital Versus Conventional Techniques for Construction of Mandibular Implant Retained Overdenture

Egypt20 participantsStarted 2022-08-20

Plain-language summary

The aim of this study is to evaluate of two different construction techniques (digital and conventional techniques) for two implant retained complete mandibular overdenture regarding: 1\. Digital occlusion stability detection: evaluated by using OccluSense. Evaluation was done in the following evaluation period: T0: Immediately after over denture insertion. T6: 6 months after over denture insertion. T12: 12 months after over denture insertion.

Who can participate

Age range

45 Years – 60 Years

Sex

MALE

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: * healthy, free from any systemic diseases relating to bone resorption such as uncontrolled diabetics or osteoporosis. * Completely edentulous jaws for at least 1 year. * The angle's class I maxillomandibular relationship and have upper and lower completely edentulous arches. * Residual alveolar ridges covered with healthy firm mucosa. * All included patients' sufficient available length and width of mandibular bone to accommodate conventional implant. (At least 5 mm buccolingual width and 12 mm vertical height of bone). Exclusion Criteria: * Patients with systemic diseases that contraindicate implant placement such as hematologic diseases * metabolic diseases related to bone resorption such as uncontrolled diabetics or osteoporosis will be also excluded * History of para-functional habits (Bruxism, clenching), smoking and alcoholism. * History of radiation therapy in the head and neck region.

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.

What they're measuring

occlusal stability

Timeframe: at time of insertion of prosthesis T(0), 6 months after insertion T(6), 12 months after insertion T(12)

Occlusal analysis

Timeframe: at time of insertion of prosthesis T(0), 6 months after insertion T(6), 12 months after insertion T(12)

Trial details

NCT IDNCT06139003

SponsorMansoura University

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2022-09-20

View on ClinicalTrials.gov More Occlusal Wear of Teeth trials