Evaluation of Autogenous Tooth- Derived Graft With Bovine Bone For Surgical Repair of Unilateral … (NCT06855875) | Clinical Trial Compass
CompletedNot Applicable
Evaluation of Autogenous Tooth- Derived Graft With Bovine Bone For Surgical Repair of Unilateral Alveolar Cleft
Egypt16 participantsStarted 2024-08-10
Plain-language summary
The aim of this study is evaluation of autogenous tooth-derived graft combined with bovine bone for surgical repair of unilateral alveolar cleft .
Who can participate
Age range
7 Years – 14 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 with unilateral alveolar clefts requiring repair.
* patients free from any systemic disease that may affect normal healing of bone.
* patients in an age 7y up to 14 y.
* patients have teeth to be sacrificed, as primary teeth, carious teeth, malposed teeth, supernumerary tooth\& non functional tooth in the study group.
Exclusion Criteria:
* Bilateral alveolar clefts.
* Immunocompromized patients.
* Syndromic patients.
* Patients have good full set of teeth, cannot be sacrified in study group
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 compared autogenous tooth-derived graft with bovine bone for repairing an alveolar cleft — can you explain what each of these materials actually is, and how they differ from the bone graft approach you're currently recommending for my child's treatment?
2The trial measured outcomes using a visual analogue scale and an inflammation score — what did those scales actually capture, and what do the results suggest about pain and swelling after surgery compared to what we might expect with a standard approach?
3Since this trial is already completed, have the full results been published anywhere, and would those findings change how you're thinking about graft material options for our specific situation?
4This was listed as a Phase NA study, which I understand often means it's a procedure or device comparison rather than a drug trial — does that affect how much confidence you have in applying these results to my child's case?
5Are there any factors in my child's individual case — like their age, the size of the cleft, or their overall health — that would make one graft material a clearly better or worse fit based on what this trial found?
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.