Socket Preservation Using Dentin Graft Autogenous Dentin Graft With Collagen Sponge on Dental Imp… (NCT06853392) | Clinical Trial Compass
CompletedPhase 3
Socket Preservation Using Dentin Graft Autogenous Dentin Graft With Collagen Sponge on Dental Implant Stability AUTOGENOUS TOOTH GRAFT WITH COLLAGEN SPONGE ON DENTAL IMPLANT STABILITY
Egypt16 participantsStarted 2023-09-15
Plain-language summary
The present study was performed to evaluate socket preservation using collagen sponge with autogenous dentin graft versus collagen sponge with de-mineralised freez-dried bone graft on dental implant stability
Who can participate
Age range
25 Years – 50 Years
Sex
FEMALE
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 are free from any systemic diseases.
* Patients with good oral hygiene.
* Age range from 25-50 years.
* Adequate inter arch space .
Exclusion Criteria:
* Medications that may affect bone turnover, and bone metabolic diseases.
* Smoker patients and alcoholics.
* Patients with parafunctional habits.
* Patients with active acute infection related to tooth of interest.
* Patients with a lack of compliance, and serious mental or psychological problems.
* Pregnant females.
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.
1This trial used a patient's own ground-up tooth (autogenous dentin graft) combined with a collagen sponge to preserve the socket after extraction — is that an approach my dentist or oral surgeon has experience with, and would it be appropriate for my specific bone loss situation?
2Since this was a Phase 3 trial that is now completed, has the data been published yet, and what did it show about changes in bone density and socket dimensions at the 6-month mark compared to other socket preservation methods?
3The trial measured bone changes using radiographic imaging over 6 months — how does that timeline and monitoring process compare to what I would go through with a standard socket preservation approach, and would I need the same number of follow-up X-rays?
4Given that this study focused on bone resorption and remodeling after tooth loss, how does my current bone density and jaw condition compare to the kinds of patients who were likely enrolled, and does that affect whether this technique might work for me?
5Are there standard socket preservation options — like synthetic bone grafts or other donor materials — that my care team would recommend I consider alongside or instead of an autogenous dentin graft approach, based on what this trial's results showed?
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
change in radiographic Socket dimensions from base line to 6 months
Timeframe: 6 months following the end of treatment
2
change in bone density from base line to 6 months
Timeframe: 6 months following the end of treatment