Vegetable Ivory Bone Material in Bone Healing Compared to Current Standard Methods of Bone Healing
- Conditions
- Bone Volume
- Registration Number
- NCT06548685
- Lead Sponsor
- Mark Stanczyk
- Brief Summary
The purpose of this research study is to evaluate whether a biobased natural vegetable ivory formulation can produce similar or better results compared to the current standard bone healing treatment.
- Detailed Description
The patient is identified and surgical site and sides reviewed. The patient is consented to have bilateral tooth extractions which are mirror images of each other either in the maxilla or mandible.
Local anesthesia is administered and attention directed to the bilateral identified teeth. Each tooth is luxated with a straight elevator and removed with a forcep with out bony removal. The sites are curetted as indicated, irrigated with normal saline irrigation , then the sterile bone graft material (allograft and vegetable ivory bone graft) are reconstituted with sterile normal saline and placed in the tooth sockets then sutures with a 3-0 gut suture. Once hemostasis is obtained and pot operative care instructions are given, the patient is monitored for 30 minutes following the procedure then discharged.
Recruitment & Eligibility
- Status
- NOT_YET_RECRUITING
- Sex
- All
- Target Recruitment
- 5
Have parallel sites from which teeth have been extracted
They are not a candidate for bone grafting or a dental implant
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Primary Outcome Measures
Name Time Method Number of participants with completely healed bone graft surgical site Six Months The number of participants who have bone volumes that match or exceed the control sites.
- Secondary Outcome Measures
Name Time Method