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Evaluation of Micro-osteoperforation on Rate of Maxillary En-masse Retraction

Evaluation of Micro-osteoperforation on Rate of Maxillary En-masse Retraction: A Randomized Controlled Trial

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03764189
Enrollment
13
Registered
2018-12-05
Start date
2019-01-31
Completion date
2020-11-30
Last updated
2018-12-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Class II Division 1 Malocclusion

Keywords

Accelerated tooth movement AND anterior segment retraction AND miniscrews AND microosteoperforation

Brief summary

accelerated anterior teeth retraction with the help of microosteoperforation procedure and miniscrews.

Detailed description

the study contains 2 groups each contains 13 subjects, A control group (anterior segment retraction with the help of miniscrews) and an intervention group ( anterior segment retraction with the help of miniscrews and microosteoperforation)

Interventions

small holes made using large round bur

Sponsors

Cairo University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Masking description

not possible as the subject will sign an informed consent and areas of microosteoperforation will be apparent

Eligibility

Sex/Gender
FEMALE
Age
16 Years to 30 Years
Healthy volunteers
Yes

Inclusion criteria

* Females with an age ranging between 16-30 years. * Malocclusion that requires bilateral extraction of the maxillary first premolars and anterior segment retraction; Angle class I mal-occlusion with bi-alveolar dental protrusions or class II division 1. * Healthy dental and periodontal condition with a good oral hygiene * Absence of degenerative conditions. * Full set of permanent dentition.

Exclusion criteria

* Medically compromised patients. * Previous orthodontic treatment * Patients suffering from any congenital, hereditary or systemic diseases or asymmetries that might have an influence on tooth movement * Chronic use of any medications affecting orthodontic tooth movement (eg: NSAIDs). * Active periodontal affection or severe gingival inflammation.

Design outcomes

Primary

MeasureTime frameDescription
Rate of En-masse retractionthree to six monthsretracting six anterior teeth

Secondary

MeasureTime frameDescription
Root resorption affecting the six anterior teeth.three to six monthsAmount of root volume loss analyzed through CBCT software
Tipping affecting the anterior teeth.three to six monthsChanges in angular measurements calculated through CBCT software
Extrusion of anterior teeththree to six monthsLinear measurement changes in the clinical height using CBCT

Countries

Egypt

Contacts

Primary ContactNashwa abdel m mohamed, master
dr.nashwa_87@live.com01020271313
Backup ContactEman m el sayed, Phd
01005289453

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026