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New treatment option for Socket Preservation
Official title Evaluation of Dentin Graft and I-PRF With and Without Vitamin C for Post-extraction Socket Preservation
ClinicalTrials.gov ID: NCT06569264
What this study is testing
- What it's testing
- The aim of the study is to evaluate radiographic ridge width change following autogenous demineralized dentin graft (ADDG) and i-PRF addition with and without vitamin C (AA) for post extraction socket preservation. The main question is: In patient with non-restorable teeth, does adding vitamin C to dentin graft and i-PRF affect the radiographic ridge width of post extraction sockets?
A plain-language read of the study's public ClinicalTrials.gov listing. The study team confirms the details.
Who can take part
Ages 18 to 65. Healthy volunteers may be eligible.
You may be able to join if
- ≥ 18 years of age.
- Single extraction of non-molar teeth with periodontally healthy adjacent teeth.
- Non-contributory medial history.
- Non- restorable teeth indicated for extraction.
- Requiring alveolar preservation after tooth extraction prior to placement of dental implant.
You likely can't join if
- Pregnant female.
- Acute infection at extraction site.
- Systemic conditions affecting healing (e.g., diabetes, medications as bisphosphonates...)
- A participant who had radiotherapy or chemotherapy.
- Psychiatric patient, or with a learning disability, or unable to give consent.
See the full eligibility criteria
- ≥ 18 years of age.
- Single extraction of non-molar teeth with periodontally healthy adjacent teeth.
- Non-contributory medial history.
- Non- restorable teeth indicated for extraction.
- Requiring alveolar preservation after tooth extraction prior to placement of dental implant.
- Participants that are eligible for immediate implantation, yet having factors that are hindering these patients from immediate placement of an implant at the time of extraction (ex: Financial related factors -...
- Cooperative patients who are willing to commit for 3 months follow up.
- Pregnant female.
- Acute infection at extraction site.
- Systemic conditions affecting healing (e.g., diabetes, medications as bisphosphonates...)
- A participant who had radiotherapy or chemotherapy.
- Psychiatric patient, or with a learning disability, or unable to give consent.
The study team makes the final eligibility decision.
Where it's taking place
- Cairo, Egypt
Questions & answers
Do participants get paid in this trial?
This listing doesn't specify compensation. Many trials still reimburse travel or offer a stipend, so it's worth asking the study team when you connect.
Is it free to join, and do I need insurance?
Searching and applying through BridgeMD is free. In clinical trials the study-related treatment and visits are generally provided at no cost to you. You usually don't need insurance to take part - confirm specifics with the study team.
How long does this study last?
The listing doesn't state an exact length. The study team walks you through the schedule and number of visits before you decide to enroll.
Who can join this trial?
This study is enrolling all sexes, 18 years to 65 years. Healthy volunteers may be eligible. The study team makes the final eligibility decision.
Where is this trial taking place?
Study sites include Cairo, Egypt. Enter your location above to see the nearest site and check your eligibility.
Explore other conditions
BridgeMD is an information and trial-matching tool - not medical advice, and not the study sponsor. Details come from ClinicalTrials.gov; the study team decides eligibility.