search
Back to results

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
Universidade de Passo Fundo
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Deficiency, Vitamin D focused on measuring Implants, Vitamin D, Osseointegration, Histomorphometric

Eligibility Criteria

25 Years - 75 Years (Adult, Older Adult)All SexesAccepts Healthy Volunteers

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

First Posted
August 17, 2017
Last Updated
November 28, 2017
Sponsor
Universidade de Passo Fundo
search

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

We'll reach out to this number within 24 hrs