Vegetable Ivory Bone Material in Bone Healing Compared to Current Standard Methods of Bone Healing

Vegetable Ivory Bone Material Study to Evaluate Whether a Biobased Natural Vegetable Ivory Formulation Can Produce Similar or Better Results Compared to Current Standard Bone Healing Treatments

Status

Not yet recruiting

Phases

Study type

Interventional

Source

ClinicalTrials.gov

Registry ID

NCT06548685

Enrollment

Registered

2024-08-12

Start date

2024-09-30

Completion date

2025-11-30

Last updated

2024-08-12

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Bone Volume

Keywords

Vegetable Ivory Bone Material

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.

Interventions

PROCEDUREBone Grafting

Bone grafting in some sites and Vegetable Ivory Grafting in Parallel sites

OTHERVegetable Derived

Tooth extraction followed by socket preservation with vegetable ivory

Study design

Allocation

NON_RANDOMIZED

Intervention model

PARALLEL

Primary purpose

HEALTH_SERVICES_RESEARCH

Masking

NONE

Eligibility

Sex/Gender

ALL

Age

21 Years to 70 Years

Healthy volunteers

Yes

Inclusion criteria

Have parallel sites from which teeth have been extracted

Exclusion criteria

They are not a candidate for bone grafting or a dental implant

Design outcomes

Primary

Measure	Time frame	Description
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.

Contacts

Primary ContactMark Stanczyk

markstanczyk@dentivia.com315-263-7976

Backup ContactMichele O'Brien, HRPP

micheleobrien@sjhsyr.org+1 315 744 1186

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026