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Vitamin D Supplementation Prior to Non-surgical Periodontal Therapy

Randomized Clinical Trial on the Effect of Vitamin D Supplement Prior to Non-surgical Periodontal Therapy: a Feasibility Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05398770
Enrollment
26
Registered
2022-06-01
Start date
2022-11-10
Completion date
2024-06-24
Last updated
2024-12-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Inflammation, Inflammation Gum, Periodontal Diseases, Periodontal Inflammation, Periodontitis, Vitamin D

Keywords

Vitamin D, 25(OH)D, Cholecalciferol, Periodontitis

Brief summary

The purpose of this study is to test the feasibility i. e. to examine all aspects necessary for the implementation of a future randomized clinical trial (RCT) that aims to determine whether non-surgical periodontal treatment can be improved by concomitant intake of vitamin D.

Detailed description

Vitamin D is believed to have anti-inflammatory and anti-bacterial properties. This is hypnotized to play a role in periodontitis. Well-designed RCTs on this theme are lacking. We therefore aim at testing a proposed study design in a pilot study, on vitamin D supplementation and its possible adjunctive effect on non-surgical periodontitis treatment (NSPT). Altogether 28 patients with a referral for treatment at the Public Dental Service Competence Center of Northern Norway (TkNN), diagnosed with periodontitis Stage I-IV, and within the ages of 20-60 years will be recruited. Participation is voluntary and based on written informed consent. The participants will randomly be allocated into two groups of equal sizes. The intervention group will receive vitamin D supplementation of 30 µg/day, and the control group will receive placebo tablets. The study is double-blinded. The participants will be instructed to take the tablets once a day for four weeks prior to the onset of the NSPT, and for two additional weeks after their first NSPT, altogether six weeks. The aim is to ensure that the vitamin D status among those who receive vitamin D supplementation is satisfactory at the start of NSPT and throughout the NSPT period. At baseline and before the start of intervention a dentist will perform a periodontal examination, including bleeding on probing (BoP), probing pocket depth (PPD), determine lost teeth, mobility, furcation involvement and radiographic bone loss. Clinical measurements in addition to data on age and sex will be obtained from the clinics (TkNN) own medical record system. The participants will also be asked to fill out a digital questionnaire about weight and height, oral hygiene, oral health, and general health. The questions in the questionnaire will be repeated at the end of follow-up, in addition to questions on the whether or not the participants have taken the tablets as prescribed, their experienced in doing so, and finally on behaviors that affect vitamin D status (taken other supplements / use of solarium / sun holidays). At baseline, at week five and at the end of the study period, gingival crevicular fluid (GCF) and blood samples from blood vessels in the arm will be sampled and analyzed for their content of vitamin D, inflammatory markers and enzymes. As a secondary outcome we also aim to assess the correlations between levels of inflammatory markers in blood and the GCF. The duration of follow-up depends on how many treatments the dentist considers the patient will need. This is part of the ordinary treatment regimen offered to this patient group. The treatment will take place over a time-period of one month. The patient is then invited to return for a check-up after 6-8 weeks. The total estimated time that each individual will be involved in the study is approximately 11-13 weeks. Once the pilot study is completed, all steps (both scientific and practical) of the trial will be evaluated in details to assess what worked / did not work / could have worked better - including recruitment, randomization, follow-up, dropout, reason for dropout, patient compliance, side effects, GCF and blood samples; including sampling storage, shipping, analysis and more. The benefits of running a feasibility trial is that it provides valuable insight and knowledge useful for designing and conducting a future high quality clinical trial on this topic. If vitamin D is confirmed to improve the effect of NSPT in a future clinical trial, improving vitamin D status in patients would be an easy to carry out means in the fight against this disease.

Interventions

DIETARY_SUPPLEMENTVitamin D supplementation (30 µg/d)

The participants will be instructed to take the tablets (vitamin D or placebo) once a day 4 weeks prior to the onset of the non-surgical periodontal treatment (NSPT), and to continue for two weeks after their first NSPT, altogether 6 weeks.

Sponsors

Public Dental Service Competence Center of Northern Norway
CollaboratorUNKNOWN
University of Tromso
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
20 Years to 60 Years
Healthy volunteers
No

Inclusion criteria

* Patients diagnosed with chronic periodontitis according to the 2017 case definition * Adults, age group 20-60 years * Periodontitis Stage I-IV (2017 definition)

Exclusion criteria

* Systemic illnesses (diabetes, osteoporosis) * Smoking * Immuno-suppressive treatment * Pregnancy * Daily vit-D supplements * Solarium * NSPT within 6 months * Local anti-microbial treatment * No natural teeth/peri implantitis

Design outcomes

Primary

MeasureTime frameDescription
Change in periodontitis status after treatment (2017 case definition)Changes from baseline at week 5Bleeding on probing (BOP)

Secondary

MeasureTime frameDescription
Change in 25(OH)D after interventionChanges from baseline at week 5Plasma concentration of 25(OH)D
Change in biomarkers (IL-1β, IL-6, IL-8, IL-12, TNFα, CRP, MCP-1, MMP) over time as response to the interventionChanges from baseline at week 5Plasma and gingival crevicular fluid concentration of biomarkers (IL-1β, IL-6, IL-8, IL-12, TNFα, CRP, MCP-1, MMP)
Change in anti-microbial peptides (LL-37, hBD-2) after interventionChanges from baseline at week 5Gingival crevicular fluid concentration of anti-microbial peptides (LL-37 and hBD-2)

Other

MeasureTime frameDescription
Change in self-reported oral health before and after treatmentChanges from baseline at end of follow-up (week 11-13)Self-reported oral health (questionnaire 5 point scale 1=bad, 5=very good)
Change in self-reported general health before and after treatmentChanges from baseline at end of follow-up (week 11-13)Self-reported general health (questionnaire 5 point scale 1=bad, 5=very good)
Correlations with biomarkers in blood compared to levels in gingival crevicular fluidCorrelation at baselineBiomarkers in blood and gingival crevicular fluid (IL-1β, IL-6, IL-8, IL-12, TNFα, CRP, MCP-1, MMP, LL-37, hBD-2)

Countries

Norway

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026