Assessment of Implants Placed in Consolidated Graft With Different Bone Drills. (NCT06477874) | Clinical Trial Compass
UnknownNot Applicable
Assessment of Implants Placed in Consolidated Graft With Different Bone Drills.
Egypt12 participantsStarted 2024-06-09
Plain-language summary
The anterior iliac crest is a popular source of bone harvest. However, when fused to the intramembranous jaw bones, it yields low-density bones that qualitatively and quantitatively endanger the fixture's stability.
In 1994, Summers first documented using the bone-condensing approach to improve the primary stability of dental implants.
This study aims to determine whether osseodensifying the consolidated mandibular bone grafts will improve implant stability and marginal bone loss
Who can participate
Age range
18 Years – 55 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
. Patients of both sexes with an age range of 18-55 years.
. Patients subjected to a successful iliac crest mandibular bone graft after segmental mandibular resection.
. A minimal ridge height of ten millimeters and a ridge width of seven millimeters.
. Healthy soft tissue coverage, with a reasonable interaction space.
Exclusion criteria
. Clinical or radiographic signs of graft infection, rejection, or massive resorption.
. The previous exposure to radiotherapy or chemotherapy.
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.