NCT05166928

Brief Summary

This clinical study will be directed to compare the effect of presence or absence of third molar on distalization of the upper posterior segment by using carriere motion appliance

Trial Health

43
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
16

participants targeted

Target at below P25 for not_applicable

Timeline
Completed

Started Jul 2021

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
unknown

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

July 10, 2021

Completed
4 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

November 10, 2021

Completed
1 month until next milestone

First Submitted

Initial submission to the registry

December 12, 2021

Completed
10 days until next milestone

First Posted

Study publicly available on registry

December 22, 2021

Completed
3 months until next milestone

Study Completion

Last participant's last visit for all outcomes

April 1, 2022

Completed
Last Updated

December 22, 2021

Status Verified

December 1, 2021

Enrollment Period

4 months

First QC Date

December 12, 2021

Last Update Submit

December 21, 2021

Conditions

Outcome Measures

Primary Outcomes (1)

  • change in upper first molar position

    using 3d cast superimposition

    Baseline to 6 months

Study Arms (2)

group 1: control group

ACTIVE COMPARATOR

will be treated using carriere motion appliance for distalization of upper buccal segment in the presence of upper third molar

Device: carriere motion appliance

group2: teste group

ACTIVE COMPARATOR

will be treated with using carriere motion appliance for distalization of upper buccal segment with upper third molar extraction or have congenital missing upper third molar

Device: carriere motion appliance

Interventions

after finished treatment with carrirere motion appliance in the two group (group 1 have upper wisdom teeth ,group 2 have not upper wisdom teeth ) the pre and post casts will be scanned and superimposed to determine amount upper molar distalization

group 1: control groupgroup2: teste group

Eligibility Criteria

Age14 Years - 22 Years
Sexall
Healthy VolunteersYes
Age GroupsChild (0-17), Adult (18-64)

You may qualify if:

  • Angle´s Class II canine relationship, at least half-unit.
  • Skeletal Class I or mild Class II relationship.
  • Upper second molars were fully erupted before starting distalization.
  • Normal or horizontal growth pattern.
  • Good oral hygiene.
  • Absence of any systemic diseases

You may not qualify if:

  • Previous orthodontic treatment. 2. Patients who required surgery to correct skeletal discrepancies (sever skeletal class11).
  • \. Patients with hyperdontia, hypodontia, or syndromic diseases. 4. Extraction or badly destructed teeth in upper arch

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

al-Azhar university

Cairo, Naser Ciry, 11765, Egypt

Location

MeSH Terms

Conditions

Overbite

Condition Hierarchy (Ancestors)

Malocclusion, Angle Class IIMalocclusionTooth DiseasesStomatognathic Diseases

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NON RANDOMIZED
Masking
DOUBLE
Who Masked
PARTICIPANT, INVESTIGATOR
Purpose
TREATMENT
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
faculty of dental medicine (Cairo-boys) AL-Azhar University

Study Record Dates

First Submitted

December 12, 2021

First Posted

December 22, 2021

Study Start

July 10, 2021

Primary Completion

November 10, 2021

Study Completion

April 1, 2022

Last Updated

December 22, 2021

Record last verified: 2021-12

Locations