Implant Site Reaction
Conditions
Brief summary
The number of patients treated in Implantology at Nantes University Hospital is 400 per year. This pilot study aims to demonstrate the efficacy of a 6-month oral cholecalciferol supplementation on osseointegration in patients requiring dental implants and presenting with vitamin D deficiency, compared to French patients who have not undergone vitamin D screening
Detailed description
This study will be conducted on patients with vitamin D deficiency or insufficiency who visit the Restorative and Surgical Dentistry Department at the Dental Care Center of Nantes University Hospital for implant surgery. The investigator will present the study to them and record their verbal non-opposition. Clinical data from before the surgery (approximately 3 months prior), during the surgery, and postoperative visits up to 3 months afterward will be included in the OSIVID study.
Interventions
None listed
Sponsors
Nantes University Hospital
Study design
Observational model
COHORT
Time perspective
PROSPECTIVE
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* Male or female patient ≥ 18 years old, candidate for dental implant placement. * with vitamin D deficiency or insufficiency: 25(OH)D \< 25 ng/L. * affiliated with a social security scheme.
Exclusion criteria
* with a local contraindication for implant placement. * under guardianship, curatorship, or legal protection * Pregnant or breastfeeding women
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| The stability of the implan | 3 months (surgery and 3 months after) | The stability of the implant measured by RFA (Resonance Frequency Analysis) |
Countries
France
Contacts
CONTACTAnne-Gaelle Chaux, MD PhD
CONTACTAlexandra Poinas, PhD
PRINCIPAL_INVESTIGATORAnne-Gaelle Chaux, MD PhD
Nantes University Hospital
Outcome results
None listed