Perioperative Oral Vitamin D3 Supplementation on Implant Osseointegration
ConditionImplant Site Reaction
Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorNantes University Hospital
About this trial
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
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
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.
Disqualifiers
with a local contraindication for implant placement.
under guardianship, curatorship, or legal protection
Pregnant or breastfeeding women
Trial population
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.
Trial design
Design model
Cohort
Time perspective
Prospective
Treatments tested in this trial
Not listed
Trial groups
60 Participants
are grouped into 1 trial groupGroup A: patient with supplementation of vitamin D3
Trial outcomes
Primary outcomes
1
The stability of the implan
The stability of the implant measured by RFA (Resonance Frequency Analysis)
Time frame
3 months (surgery and 3 months after)Sponsors and contacts
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Source ClinicalTrials.gov