ClinicalTrials.gg
CompletedNCT05599074Updated Nov 9, 2022

Stability of Anterior Open Bite Treatment Using Extrusion Arches

An interventional study of extrusion arch in Anterior Open Bite Malocclusion, sponsored by Alexandria University. Completed at 1 site in Egypt. Open to participants aged 18 Years to 40 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2022-11-09.

Primary conditionOpen BiteRegistry: MalocclusionReclassifiedWhy we changed it
Registry
Malocclusion — the first condition term the registry derived for this study.
ClinicalTrials.gg
Open Bite
Why
  1. The study's listed conditions name Open Bite, a narrower term within Malocclusion.
Confidence
High: the new condition is named in the study's own listed conditions. Of 351 hand-checked studies reclassified this way, 68% were exactly right and 84% in the right disease family; the registry's first term was right for 5% (measured 2026-10-21). How we classify →
Wrong?
Tell us the study's main condition →

Sponsored by Alexandria University · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Registered 3 years 6 months after the study started (first participant enrolled Apr 2019, registered Oct 2022).
Phase
Not applicable
Study type
Interventional
Enrollment
23
Allocation
Not applicable
Ages
18 Years to 40 Years
Sex
All
01

Study summary

This study investigated treatment effects and stability of anterior open bite cases using extrusion arches

02

Conditions studied

  • Anterior Open Bite Malocclusion

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Keywords

  • extrusion arches
  • anterior open bite
  • stability
  • extrusion
  • intrusion
03

In context

Open Bite Reclassified

34 studies on the registry are indexed under Open Bite; 8 are open to participants now.

This study's enrollment of 23 is below the median of 30 across 28 interventional studies indexed under Open Bite.

Browse Open Bite studies →

Lead sponsor

Alexandria University is the lead sponsor of 604 studies on the registry; 140 are open to participants now.

Of its 13 completed or terminated interventional studies of FDA-regulated products, 0 (0%) have results posted.

Compared within Open Bite, this study's primary condition as ClinicalTrials.gg classifies it; the registry's first condition term is Malocclusion. The counts are of registry records indexed under each term, refreshed daily. How we classify →

04

Who can participate

Ages eligible
18 Years to 40 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • adult patients above 18 years anterior open bite 2-6 mm full permanent dentition incisors requiring extrusion

Exclusion criteria

Exclusion Criteria:

  • increased incisal show at rest
  • gum show at smiling cleft patients patient with tempro-mandibular joint problems FMA angle above 45
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
23 participants (actual)

Study arms

  • Experimental
    AOB adults

    adult patients over 18 years having an anterior open bite of more than 2 mm, requiring incisors extrusion

    Device: extrusion arch

Interventions

  • Deviceextrusion arch

    A stainless steel pre-formed arch wire custom made by placing V-bends 3-5 mm mesial to the molar tubes, placed into the auxiliary molar tubes after leveling phase and tied over the main arch wire distal to the lateral incisors

06

What researchers measure

Primary outcomes

  1. SNA angle

    The anteroposterior position of maxillary base to the anterior cranial base.

    Time frame: 18 months

  2. SNB angle

    The anteroposterior position of mandibular base to the anterior cranial base.

    Time frame: 18 months

  3. ANB angle

    The anteroposterior position of maxillary base to the mandibular base.

    Time frame: 18 months

  4. SN-MP angle

    Mandibular plane angle, the angle between the mandibular plane (Go-Me) and anterior cranial base plane (SN).

    Time frame: 18 months

  5. PP-MP angle

    The angle between palatal plane (ANS-PNS) and mandibular plane.

    Time frame: 18 months

  6. AFH

    Anterior facial height, the measurement between Nasion (N) and Menton (Me).

    Time frame: 18 months

  7. interincisal angle

    - The inner angle between the long axis of the maxillary central incisor and long axis of mandibular central incisor.

    Time frame: 18 months

  8. L1 to MP in mm

    - The perpendicular distance between the most anterior mandibular central incisor and mandibular plane.

    Time frame: 18 months

  9. L1 to MP angle

    The angle between long axis of the most anterior central incisor and the mandibular plane.

    Time frame: 18 months

  10. overbite

    Vertical distances between the incisal edges of the maxillary and mandibular central incisors, perpendicular to N-Me.

    Time frame: 18 months

  11. U1 to PP angular and linear measurements

    -The angle and perpendicular distance between long axis of the most anterior upper central incisor and the Palatal plane (ANS-PNS).

    Time frame: 18 months

  12. u6 to pp angle

    -The angle between the axis between mesial cusp tip and mesiobuccal root apex of the upper first molar and the palatal plane.

    Time frame: 18 months

  13. U6 to PP in mm

    -The perpendicular distance between the mesial cusp tip of the upper first maxillary molar and the palatal plane.

    Time frame: 18 months

  14. L6 to MP angle

    The angle between the axis between mesial cusp tip and mesial root apex of the lower first molar and the mandibular plane.

    Time frame: 18 months

  15. L6 to MP in mm

    The perpendicular distance between mesial cusp tip of the lower first molar and the mandibular plane.

    Time frame: 18 months

07

Study locations

1 site
  • Alexandria faculty of Dentistry
    Alexandria, 21589, Egypt
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Nov 9, 2022, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT05599074
Responsible party
Tasnim Yousry (Ms, Alexandria University) — Principal investigator
First posted
Oct 31, 2022
Start date
Apr 1, 2019
Primary completion
May 1, 2022
Completion
May 1, 2022
Last update
Nov 9, 2022

Study contacts

tasneem hammad, BDS
principal investigator · Alexandria University
hanan ismail, PHD
study director · Alexandria University

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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This study is completed, as verified in Nov 2022. You cannot join it, but the record below documents what was studied.

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