Clinical and Radiographic Evaluation of Delayed Dental Implant Placement After Socket Preservatio… (NCT07373600) | Clinical Trial Compass
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Clinical and Radiographic Evaluation of Delayed Dental Implant Placement After Socket Preservation Using Injectable Bone Graft
20 participantsStarted 2026-01
Plain-language summary
This clinical study aims to evaluate the clinical and radiographic outcomes of delayed dental implant placement following socket preservation using an injectable alloplastic bone graft material.
The study will include patients who require tooth extraction and are candidates for implant placement.
After tooth extraction, the socket will be preserved using the bone graft material, and dental implants will be placed after a healing period.
Clinical and radiographic assessments will be performed to evaluate bone quality, bone height, and implant stability.
The goal of this study is to determine the effectiveness of injectable alloplastic bone grafts in maintaining the alveolar ridge and improving the success of delayed implant placement.
Who can participate
Age range
40 Years – 60 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.
* Patient aged between 40 and 60 years
* General good health.
* Volunteer subjects have to voluntarily sign an informed consent.
* Patient Indicated for single implant placement in lower posterior area.
Inclusion criteria for patients in group I
· Patient with a previously extracted lower posterior tooth and the socket was preserved with injectable bone graft .
Exclusion criteria:
* Patient with systemic disease affection bone metabolism .
* Patients with contraindication to surgical treatment.
* Patients with uncontrolled medical conditions.
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
1
Implant stability at the time of delayed implant placement
Timeframe: At the time of delayed implant placement (approximately 4 to 6 months after tooth extraction)