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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04020952
Other study ID # 334
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date September 10, 2019
Est. completion date July 15, 2021

Study information

Verified date July 2022
Source Cairo University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

trial will be done to evaluate the effect of archwire gauge on the rate of canine retraction, canine tip and torque, root resorption and loss of anchorage in maxillary dental protrusion cases requiring first premolars extraction.


Description:

Three working archwires of different gauges will be used during canine retraction; st.st 0.019×0.025" as a comparator, st.st 0.016×0.022" and st.st 0.017×0.025" wires as interventions. after levelling and alignment till reaching the working archwire, it will be left in place for a month then maxillary first premolars will be extracted and base line records will be taken(digital models, digital periapical radiographs and panorama). digital models will be taken monthly to measure rate of canine retraction for 6 months. after 6 month evaluation of anchorage loss, change in canine tip and torque will be done on last obtained digital model , panorama will be taken to evaluate the change in canine tip and digital periapical radiograph will be taken and compared with the preretraction radiograph to evaluate amount of root resorption.


Recruitment information / eligibility

Status Completed
Enrollment 18
Est. completion date July 15, 2021
Est. primary completion date September 20, 2020
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 16 Years to 26 Years
Eligibility Inclusion Criteria: - Adult females (age range 18-28 years old). - Maxillary dental protrusion indicating first premolars extraction. - Full permanent dentition (not necessitating third molars). Exclusion Criteria: - Patients having systemic diseases or on medications that would affect tooth movement. - Active periodontal disease or obvious bone resorption in maxillary arch. - Patients with habits that are detrimental to dental occlusion (thumb sucking, tongue thrusting … etc.). - Previous orthodontic treatment. - Missing teeth.

Study Design


Related Conditions & MeSH terms


Intervention

Other:
st.st 0.019×0.025" wire
rectangular stainless steel wire that will be used during canine retraction after first premolars extraction
st.st 0.016×0.022" wire
rectangular stainless steel wire that will be used during canine retraction after first premolars extraction
st.st 0.017×0.025" wire
rectangular stainless steel wire that will be used during canine retraction after first premolars extraction

Locations

Country Name City State
Egypt faculty of dentistry, Cairo University Cairo

Sponsors (1)

Lead Sponsor Collaborator
Cairo University

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary rate of canine retraction the distance that canine moved every month 6 months
Secondary change in canine tip change in canine crown tipping to certain reference plane with the aid of cone beam computed tomography 6 months
Secondary change in canine torque change in canine crown and root torque to certain reference plane with the aid of cone beam computed tomography 6 months
Secondary loss of molar anchorage assess from digital models if there is change in mesio-distal position of maxillary first molar 6 months
Secondary amount of canine root resorption assess amount of root resorption (if occurred) with the aid of cone beam computed tomography 6 months
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Active, not recruiting NCT05727124 - Poul Gjessing Versus T Loops for Orthodontic Maxillary Canine Retraction N/A
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