Efficacy of Perioperative Oral Vitamin D3 Supplementation on Implant Osseointegration in Patients With Vitamin D Deficiency
Status: Recruiting
Location: See location...
Study Type: Observational
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
Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:
• 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.
Locations
Other Locations
France
CHU Nantes-Department of Dentistry
RECRUITING
Nantes
Contact Information
Primary
Anne-Gaelle Chaux, MD PhD
annegaelle.chaux@chu-nantes.fr
02 53 48 28 35
Backup
Alexandra Poinas, PhD
alexandra.poinas@chu-nantes.fr
0253482857
Time Frame
Start Date: 2025-01-15
Estimated Completion Date: 2027-05-15
Participants
Target number of participants: 60
Treatments
patient with supplementation of vitamin D3
perioperative oral vitamin D3 supplementation on implant osseointegration in patients with vitamin D deficiency.
Related Therapeutic Areas
Sponsors
Leads: Nantes University Hospital