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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03260829
Other study ID # oral and dental medicine
Secondary ID no conflict of i
Status Completed
Phase N/A
First received January 11, 2017
Last updated August 25, 2017
Start date January 2014
Est. completion date February 2015

Study information

Verified date August 2017
Source Cairo University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

efficacy of the injectable vitamin C to reduce the time of canine traction


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.


Recruitment information / eligibility

Status Completed
Enrollment 12
Est. completion date February 2015
Est. primary completion date January 2015
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 15 Years to 40 Years
Eligibility 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 a 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).

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
vitamin C
25 IU of vitamin C injected intraepidermally for 6-8 visits till eruption achieved

Locations

Country Name City State
Egypt Faculty of Oral and Dental Medicine Gizah Giza

Sponsors (1)

Lead Sponsor Collaborator
Cairo University

Country where clinical trial is conducted

Egypt, 

References & Publications (1)

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. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary rate of tooth movement the achieved movement in millimeters in one year 12 months
Secondary level of alveolar bone the level of the interproximal and facial alveolar bone after orthodontic treatment with or without injection 12 months
See also
  Status Clinical Trial Phase
Completed NCT01093352 - Effect of Alveolar-decortication on Velocity of Tooth Movement N/A