Efficacy of Injectable Vitamin C on Accelerating Canine Movement: A Clinical Study (mesotherapy)
Primary Purpose
Palatally Impacted Canines
Status
Completed
Phase
Not Applicable
Locations
Egypt
Study Type
Interventional
Intervention
vitamin C
Sponsored by
About this trial
This is an interventional treatment trial for Palatally Impacted Canines focused on measuring vitamin C, palatally impacted canines, intraepidermal injection
Eligibility Criteria
Inclusion Criteria:
- medically free
- patient with good to fair oral hygiene (gingivitis may be included)
- both sexes were included
- unilateral palatally positioned permenant canines
- absence of previous orthodontic treatment
- absence of supernumerary teeth, odontoms, cysts, traumatic injuries
- the α angle within grade II to III
Exclusion Criteria:
- systemic diseases especially diabetes and bone diseases
- pregnant and lactating mothers
- Local causes (smoking, mouth breathing, local trauma and periodontitis).
Sites / Locations
- Faculty of Oral and Dental Medicine
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Placebo Comparator
Arm Label
vitamin C injection
orthodontic traction
Arm Description
orthodontic traction with vitamin C injection
orthodontic traction without vitamin C injection
Outcomes
Primary Outcome Measures
rate of tooth movement
the achieved movement in millimeters in one year
Secondary Outcome Measures
level of alveolar bone
the level of the interproximal and facial alveolar bone after orthodontic treatment with or without injection
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT03260829
Brief Title
Efficacy of Injectable Vitamin C on Accelerating Canine Movement: A Clinical Study
Acronym
mesotherapy
Official Title
Evaluation of the Effect of Local Injected Vitamin C on Accelerating the Orthodontic Movement of Maxillary Canine Impaction: A Clinical Trial
Study Type
Interventional
2. Study Status
Record Verification Date
August 2017
Overall Recruitment Status
Completed
Study Start Date
January 2014 (undefined)
Primary Completion Date
January 2015 (Actual)
Study Completion Date
February 2015 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Cairo University
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
No
5. Study Description
Brief Summary
efficacy of the injectable vitamin C to reduce the time of canine traction
Detailed Description
Objective. The purpose of this study is to investigate the role and efficiency of the locally injected vitamin C in the enhancement of the palatally impacted canine movement.
Design. Twelve adult patients with unilateral palatally impacted canines were included in this study. The enrolled patients were randomly allocated into the study groups; control group; orthodontic traction and he test group: orthodontic traction enhanced by intraepidermic vitamin C injection. The study duration was 12 months.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Palatally Impacted Canines
Keywords
vitamin C, palatally impacted canines, intraepidermal injection
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Participant
Allocation
Non-Randomized
Enrollment
12 (Actual)
8. Arms, Groups, and Interventions
Arm Title
vitamin C injection
Arm Type
Active Comparator
Arm Description
orthodontic traction with vitamin C injection
Arm Title
orthodontic traction
Arm Type
Placebo Comparator
Arm Description
orthodontic traction without vitamin C injection
Intervention Type
Drug
Intervention Name(s)
vitamin C
Other Intervention Name(s)
ascorbic acid
Intervention Description
25 IU of vitamin C injected intraepidermally for 6-8 visits till eruption achieved
Primary Outcome Measure Information:
Title
rate of tooth movement
Description
the achieved movement in millimeters in one year
Time Frame
12 months
Secondary Outcome Measure Information:
Title
level of alveolar bone
Description
the level of the interproximal and facial alveolar bone after orthodontic treatment with or without injection
Time Frame
12 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
15 Years
Maximum Age & Unit of Time
40 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
medically free
patient with good to fair oral hygiene (gingivitis may be included)
both sexes were included
unilateral palatally positioned permenant canines
absence of previous orthodontic treatment
absence of supernumerary teeth, odontoms, cysts, traumatic injuries
the α angle within grade II to III
Exclusion Criteria:
systemic diseases especially diabetes and bone diseases
pregnant and lactating mothers
Local causes (smoking, mouth breathing, local trauma and periodontitis).
Facility Information:
Facility Name
Faculty of Oral and Dental Medicine
City
Gizah
State/Province
Giza
ZIP/Postal Code
11311
Country
Egypt
12. IPD Sharing Statement
Citations:
PubMed Identifier
1
Citation
Makar AB, McMartin KE, Palese M, Tephly TR. Formate assay in body fluids: application in methanol poisoning. Biochem Med. 1975 Jun;13(2):117-26. doi: 10.1016/0006-2944(75)90147-7. No abstract available.
Results Reference
result
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Efficacy of Injectable Vitamin C on Accelerating Canine Movement: A Clinical Study
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