Autogenous Tooth Bone Graft for Alveolar Socket Preservation (NCT07267637) | Clinical Trial Compass
Active — Not RecruitingNot Applicable
Autogenous Tooth Bone Graft for Alveolar Socket Preservation
Yemen20 participantsStarted 2024-07-14
Plain-language summary
The purpose of this clinical experiment is to assess how well autogenous tooth bone grafting preserves the alveolar socket after surgical tooth extraction. Before being inserted into the socket, the graft is made from the patient's own extracted tooth and ground into a particle. Twenty Yemeni patients who needed their teeth extracted are included in the trial, and they will be followed up with clinical and radiographic procedures using cone-beam computed tomography (CBCT) for six months. The primary objective is to ascertain whether the autogenous dental bone graft can preserve the height, width, and density of alveolar bone, offering a secure, affordable, and biocompatible substitute for traditional grafting materials.
Who can participate
Age range
18 Years – 40 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:
* \- Absence of systemic diseases.
* Very good to accepted oral hygiene.
* Patients with impacted teeth requiring extraction.
* Patients between the ages of 16 and 50.
* No history of smoking.
* No history of any other drug use.
* Patients who were cooperative, motivated, to attend the follow-up and maintenance visits.
Exclusion Criteria:
* Systemic conditions or pharmacological therapies that could be an absolute contraindication for the intervention (such as un controlled diabetics, immunocompromised states, or treatment with oral or parenteral bisphosphonates).
* Poor oral hygiene.
* Acute exacerbation of chronic infection like pain or swelling.
* Pregnant women, children, elderly (\>60 years), physically and mentally challenged, terminally and seriously ill.
* Hight Smoking tendency.
* Patients who refused to participate in the trial.
* Uncooperative Patients who won't be able to maintain the follow up visits
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
"Alveolar Bone Height, Width, and Density Preservation with Autogenous Tooth Bone Graft"
Timeframe: "Before extraction and 6 months post-intervention"