Effect of Vitamin D Replacement on Bone Healing in Mini-dental Implants
Primary Purpose
Deficiency, Vitamin D
Status
Unknown status
Phase
Phase 1
Locations
Brazil
Study Type
Interventional
Intervention
Vitamin D
Placebo
Sponsored by
About this trial
This is an interventional treatment trial for Deficiency, Vitamin D focused on measuring Implants, Vitamin D, Osseointegration, Histomorphometric
Eligibility Criteria
Inclusion Criteria:
- Patients of both sexes;
- No medical, temporary or intra-oral contraindications;
- Good general health;
- Need of implant in the maxilla in the posterior region (with a minimum of 5 mm of bone height visualized radiographically) or in mandible in posterior region;
- With vitamin D deficiency / deficiency (considering serum level of ≥ 15 ng / ml at ≤ 25 ng / ml).
Exclusion Criteria:
- Medical, temporary or intrabuccal contraindications;
- Smokers;
- Use of corticoid;
- Post-operative of bariatric surgery;
- Bone height less than 5mm;
- Need for maxillary sinus lift;
- Vitamin supplementation D.
Sites / Locations
- Isadora RinaldiRecruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Placebo Comparator
Arm Label
Arm vitamin D
Arm placebo
Arm Description
Vitamin D 5.000 IU a day for 2 months (10 drops after lunch)
Placebo for 2 months (10 drops after lunch)
Outcomes
Primary Outcome Measures
Percentage of bone implant contact
Histomorphometry will be used as a method of analysis. It will evaluate the initial stage of osseointegration in the two groups, relating it to insufficiency / deficiency and sufficiency of vitamin D. The percentage of bone implant contact, defined as the amount of mineralized bone in direct contact with the surface of the miniimplant, will be evaluated.
Secondary Outcome Measures
Serum levels of vitamin D (ng/ml)
The 25-hydroxyvitamin D test is a common blood test and is the best way to monitor vitamin D levels. The test can determine if the person's blood has deficiency or excessive vitamin D. The method used to evaluate the blood test is chemiluminescent immunoassay technology (CLIA).
Full Information
NCT ID
NCT03356730
First Posted
August 17, 2017
Last Updated
November 28, 2017
Sponsor
Universidade de Passo Fundo
1. Study Identification
Unique Protocol Identification Number
NCT03356730
Brief Title
Effect of Vitamin D Replacement on Bone Healing in Mini-dental Implants
Official Title
Effect of Vitamin D Replacement on Bone Healing in Mini-dental Implants: a Randomized Clinical Trial
Study Type
Interventional
2. Study Status
Record Verification Date
November 2017
Overall Recruitment Status
Unknown status
Study Start Date
November 19, 2017 (Actual)
Primary Completion Date
December 30, 2017 (Anticipated)
Study Completion Date
April 30, 2018 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Universidade de Passo Fundo
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
Title
Executive team
Research line
Summary
Research problem
Justification
Literature review
Objectives
Materials and methods
Dissemination of knowledge generated
Schedule of activities
Budget
References
Annexes
Detailed Description
This is a clinical research study, characterized by a randomized, double-blind, placebo-controlled clinical trial. Background: Vitamin D replacement could aid in the osseointegration of dental implants. Objective: to evaluate the effect of vitamin D replacement on osseointegration of dental implants in humans. Materials and methods: Twenty individuals with hypovitaminosis D underwent dental miniimplants and randomized to two equal groups for treatment with vitamin D (5000 IU / day) or placebo for 2 months. After two months, the miniimplants will be removed and prepared for histomorphometric analysis, which will evaluate bone implant contact in percentage. Testing the hypothesis that the contact between bone and implant and the bone density in the threaded area in the test group is higher than in the control group. Test t will be used to compare the differences between the groups.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Deficiency, Vitamin D
Keywords
Implants, Vitamin D, Osseointegration, Histomorphometric
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 1
Interventional Study Model
Parallel Assignment
Model Description
This is a clinical research study, characterized by a randomized, double-blind, placebo-controlled trial.
Masking
ParticipantInvestigator
Masking Description
Masking for placebo or vitamin D use
Allocation
Randomized
Enrollment
20 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Arm vitamin D
Arm Type
Experimental
Arm Description
Vitamin D 5.000 IU a day for 2 months (10 drops after lunch)
Arm Title
Arm placebo
Arm Type
Placebo Comparator
Arm Description
Placebo for 2 months (10 drops after lunch)
Intervention Type
Drug
Intervention Name(s)
Vitamin D
Intervention Description
Only patients with vitamin D deficiency / deficiency will be included in the study. Randomly, they will be divided into two groups. This group will receive vitamin D supplementation.
Vitamin D3 - cholecalciferol, oral suspension in drops, will be prescribed as follows:
• 5,000 IU / day - 10 drops per day for two months.
Intervention Type
Other
Intervention Name(s)
Placebo
Intervention Description
Only patients with vitamin D deficiency / deficiency will be included in the study. Randomly, they will be divided into two groups. This control group will receive placebo.
Placebo (olive oil mint flavor), oral suspension in drops, will be prescribed as follows:
• 10 drops per day for two months.
Primary Outcome Measure Information:
Title
Percentage of bone implant contact
Description
Histomorphometry will be used as a method of analysis. It will evaluate the initial stage of osseointegration in the two groups, relating it to insufficiency / deficiency and sufficiency of vitamin D. The percentage of bone implant contact, defined as the amount of mineralized bone in direct contact with the surface of the miniimplant, will be evaluated.
Time Frame
2 months
Secondary Outcome Measure Information:
Title
Serum levels of vitamin D (ng/ml)
Description
The 25-hydroxyvitamin D test is a common blood test and is the best way to monitor vitamin D levels. The test can determine if the person's blood has deficiency or excessive vitamin D. The method used to evaluate the blood test is chemiluminescent immunoassay technology (CLIA).
Time Frame
2 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
25 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
Patients of both sexes;
No medical, temporary or intra-oral contraindications;
Good general health;
Need of implant in the maxilla in the posterior region (with a minimum of 5 mm of bone height visualized radiographically) or in mandible in posterior region;
With vitamin D deficiency / deficiency (considering serum level of ≥ 15 ng / ml at ≤ 25 ng / ml).
Exclusion Criteria:
Medical, temporary or intrabuccal contraindications;
Smokers;
Use of corticoid;
Post-operative of bariatric surgery;
Bone height less than 5mm;
Need for maxillary sinus lift;
Vitamin supplementation D.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Isadora Rinaldi
Phone
(54) 9 9696-8365
Email
120910@upf.br
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Maria Salete Sandini Linden
Organizational Affiliation
Universidade de Passo Fundo
Official's Role
Study Director
Facility Information:
Facility Name
Isadora Rinaldi
City
Rondinha
State/Province
Rio Grande Do Sul
ZIP/Postal Code
99590-000
Country
Brazil
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Isadora Rinaldi, Miss
Phone
54996968365
Email
120910@upf.br
12. IPD Sharing Statement
Plan to Share IPD
Yes
IPD Sharing Plan Description
The individual participants data (IPD) will be available in the dental records including complementary exams, allowing the access of other researchers during the research.
Learn more about this trial
Effect of Vitamin D Replacement on Bone Healing in Mini-dental Implants
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