Vit D: to address the relation between Vitamin D deficiency and Dental implant osseointegration for the identification of the participants whom may be non-responders to the vitamin D treatment
Study summary
The primary goal for any oral implantologist is to obtain satisfactory healing and long-term treatment success. Osseointegration is the key to dental implant success8 and is required to achieve direct structural and functional connection between living bone and the surface of a load-bearing artificial implant, is critical for the long-term success of dental implants.
Successful dental implant therapy relies on achieving proper osseointegration, which ensures a stable structural and functional bond between the implant surface and surrounding bone. Although dental implants show a high overall success rate of around 95%.
Eligibility
Sex
ALL
Min age
20 Years
Max age
60 Years
Healthy volunteers
Accepted
Inclusion Criteria:
* Adults aged 20-60 with diagnosed vitamin D deficiency (\<20 ng/mL).
* Edentulous area in the posterior mandible or maxilla.
* No history of previous dental implant failure, metabolic bone diseases, or conditions affecting bone healing.
* Both genders are included
Exclusion Criteria:
* Severe systemic diseases that could interfere with healing.
* Patients already on vitamin D or calcium supplements.
* Smokers or patients with poor oral hygiene practices.
* Pregnant females
Primary outcome measure(s)
Treatment of Dental Implant Osseointegration — 3 Months Evaluation of the Primary implant stability measured immediately after implant placement using the Ostell device, which assesses resonance frequency analysis (RFA) values expressed as Implant Stability Quotient (ISQ). This measurement reflects the initial mechanical stability of the implant within the bone at the time of surgery.
marginal bone loss after prosthesis placement — six months after proshtesis placement Marginal bone loss will be evaluated using cone beam computed tomography (CBCT) taken six months after prosthesis placement. The vertical distance between the implant shoulder and the first bone-to-implant contact will be measured on both mesial and distal aspects to assess the amount of peri-implant bone resorption over time.
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
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