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NCT Number: NCT06497244

Evaluation of the Effect of Micro-osteoperforation on the Rate of Bone Anchored Molar Distalization

The primary aim of the current study was to evaluate three dimensionally, using digital models and cone beam computed tomography imaging, the effect of micro-osteoperforations on the rate of tooth movement in the first molar distalization.

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Key information

Age range

16 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Cairo university

Cairo, Egypt

Location status: Recruiting

Location contact

faculty of dentistry Cairo university

CONTACT

0020223634965

About this study

The design of this randomized controlled clinical trial is a parallel group, two arms trial

  • Preparatory phase
  • Self-drilling mini-screws will be placed buccally between upper 2nd premolar and 1st molar bilaterally in the last NiTi wire insertion visit.
  • After the completion of levelling and alignment phase an intra oral scan will be made for the upper arch and a rigid stainless-steel retraction arch wire 0.017" x 0.025" will be inserted.
  • The patient will then be referred to the radiology center and a pre-retraction cone beam computed tomography (CBCT) image will be taken for the maxillary arch (T0).
  • Experimental phase
  • Subjects will receive MOPs randomly to either the left or right maxillary molar buccal alveolar regions. MOPs will be performed at the first day of the distalization treatment (T0) and will repeated every 2 months.
  • Molar distalization will started immediately after performing the MOPs using sliding jig distalizer.
  • The force will be applied to the mini-screw with the sliding jig mechanics on average 300 gm using Nickel-titanium closing coil springs.
  • Before leaving the clinic, the patient will be asked to:
  • Use chlorhexidine three times per day for 3 days after MOP applications.
  • avoid using pain killers (except Panadol when needed).
  • fill in a Numeric pain rating scale.
  • Follow up phase
  • Follow up visits will be scheduled every 4 weeks for reactivation coil spring and check TADs stability.
  • An intra oral scan for the upper arch will made every visit.
  • The study time will be continued for 6 months (T1, T2, T3, T4, T5, T6).
  • The same technique of MOP will be repeated after 2 and 4 months of follow up (T2,T4).
  • After 6 months of follow up, the final dental model will made, and the patient will be referred to the same radiology center to acquire the post-distalization CBCT.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Adult patients
  • Skeletal Class I or mild Class II relationship
  • Dental class II bilaterally (non-extraction cases)
  • Full permanent dentition including 2nd maxillary molars
  • Good oral hygiene
  • Medically free

Exclusion criteria

  • Systemic diseases that may interfere with the treatment
  • Use of any medications that might have affected the biology of tooth movement
  • unilateral Class II molar relationship
  • extreme skeletal Class II relationship (ANB >7°)
  • periodontal disease or alveolar bone loss
  • Patients with dental anomalies in maxillary 1st molar

Treatment and study plan

micro osteo-perforation

Procedure

the patient will receive miniscrew micro osteo-perforation in one side every month with molar distalization and the other side the distalization without micro osteo-perforation

Primary outcomes

  1. rate of molar distalization

    Time frame: 6 months

    Incremental rate of molar distalization every month by intra oral scan superimposition

  2. total molar distalization distance by mm between T6 and T0

    Time frame: 6 months

    Total distance moved by the molar after 6 months by intra oral scan superimposition and measure the linear difference in position 1st molar between T6 and T0 by mm

Secondary outcomes

  1. The effect of MOPs on Maxillary 1st molar tipping by degrees between T6 and T0

    Time frame: 6 months

    comparing the pre- & post- distalization CBCT and measure the angular change in the 1st molar long axis tipping by degree between T6 and T0

  2. The effect of MOPs on Maxillary 1st molar rotation by degrees between T6 and T0

    Time frame: 6 months

    comparing the pre- & post- distalization digital models and CBCT and measure the angular change in the 1st molar long axis rotation by degree between T6 and T0

  3. The effect of MOPs on Maxillary 1st molar vertical movement by mm between T6 and T0

    Time frame: 6 months

    comparing the pre- & post- distalization CBCT and measure the linear change in the 1st molar vertical position by mm between T6 and T0

  4. The effect of MOPs on 1st molar root resorption level by mm between T6 and T0

    Time frame: 6 months

    comparing the pre- & post- distalization CBCT and measure the amount of root resorption of 1st molar roots by mm between T6 and T0

  5. Detecting any Pain or discomfort caused by the micro-osteoperforations using Numeric pain rating scale

    Time frame: 1 week

    using Numeric Pain Rating Scale filled by the patient with minimum value is zero and maximum value 10 (the higher score mean worse outcome)

Study contacts

Contact information is provided by the study sponsor or research team.

Mohamed Elsayed, PhD

CONTACT

[email protected]

00201064111810

Sponsors and collaborators

Lead sponsor

Cairo University

Other

Registry information

Official study title

Evaluation of the Effect of Micro-osteoperforation on the Rate of Bone Anchored Molar Distalization: a Split-mouth Randomized Controlled Clinical Trial

Important dates

Study start
2023
Primary completion
2024
Study completion
2024
First posted
Jul 11, 2024
Registry last updated
Jul 12, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.