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The Effect of Different Force Magnitudes on Maxillary Posterior Segment Intrusion

The Effect of Two Different Force Magnitudes on Maxillary Posterior Segment Intrusion in Adult Patients With Skeletal Open Bite Using Temporary Anchorage Devices- A Randomized Clinical Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02901678
Enrollment
20
Registered
2016-09-15
Start date
2015-11-30
Completion date
2018-04-30
Last updated
2018-08-02

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

Conditions

Orthodontics

Keywords

skelatal open bite, posterior intrusion

Brief summary

A Randomized clinical trial comparing two different force magnitudes in maxillary posterior segment intrusion in adult patients with skeletal open bite malocclusion

Detailed description

This randomized controlled trial is aiming to study the effect of the different force magnitude on maxillary posterior segment intrusion. Two groups are going to be allocated and the amount and rate of intrusion will be measured and compared.

Interventions

DEVICEIntrusion by 400 g

using miniscrews and coil springs to apply the intrusive force on maxillary posterior segment intrusion.

Sponsors

Cairo University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
15 Years to 25 Years
Healthy volunteers
Yes

Inclusion criteria

* Adult patients with an age range from 17 to 25. * Skeletal open bite. * Dental open bite that is due to overgrowth of maxillary posterior segment as seen clinically and that can be corrected without surgical intervention (a minimum of 3 mm and a maximum of 8 mm). * Skeletal class I or mild to moderate skeletal class II that enables camouflage treatment. * Normal incisor show on smiling (that makes the case indicated for molar intrusion and not for incisor extrusion). * Full set of maxillary posterior dentition (first and second premolars, first molars at least). * No previous orthodontic treatment.

Exclusion criteria

* Medically compromised patients. * Patients suffering from any congenital or hereditary diseases. * Smoking or any systemic diseases. * Chronic use of any medications including antibiotics, phenytoin, cyclosporin, anti-inflammatory drugs, systemic corticosteroids, and calcium channel blockers.

Design outcomes

Primary

MeasureTime frameDescription
Amount of intrusion6 monthsThe amount the upper posterior teeth have been intruded.
Rate of bite closure6 monthsThe rate by which the open bite closes as a result of posterior segment intrusion

Secondary

MeasureTime frameDescription
Average rate of intrusion6 monthsThe amount of intrusion divided by the duration of intrusion
Root resorption6 monthsThe amount of root resorption as a result of the intrusive force
Tipping6 monthsThe amount of mesiodistal and buccolingual tipping of posterior teeth

Countries

Egypt

Outcome results

None listed

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