NCT06467240

Brief Summary

This study will be directed for Evaluation of the hybrid rapid maxillary expander assisted with Micro-osteo perforation (MOPs) in adults

Trial Health

87
On Track

Trial Health Score

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

Enrollment
14

participants targeted

Target at below P25 for all trials

Timeline
Completed

Started Oct 2024

Shorter than P25 for all trials

Geographic Reach
1 country

1 active site

Status
completed

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

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

May 19, 2024

Completed
1 month until next milestone

First Posted

Study publicly available on registry

June 20, 2024

Completed
3 months until next milestone

Study Start

First participant enrolled

October 1, 2024

Completed
8 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

June 1, 2025

Completed
3 months until next milestone

Study Completion

Last participant's last visit for all outcomes

August 20, 2025

Completed
Last Updated

September 8, 2025

Status Verified

August 1, 2025

Enrollment Period

8 months

First QC Date

May 19, 2024

Last Update Submit

August 30, 2025

Conditions

Keywords

maxillary expansionMicro-osteo perforationCross Bite

Outcome Measures

Primary Outcomes (2)

  • CBCT measurment

    amount of skeletal and dental expansion

    3 weeks

  • suture opening

    amount of skeletal and dental expansion

    3 weeks

Study Arms (2)

intervention group

will receive a hybrid rapid maxillary expander assisted by Micro-osteo perforation (MOPs) in mid palatine suture

Procedure: hybrid rapid maxillary expander assisted with Micro-osteo perforation (MOPs)

control group

will receive a hybrid rapid maxillary expander without any thing

Procedure: hybrid rapid maxillary expander assisted with Micro-osteo perforation (MOPs)

Interventions

patients with constricted maxillary will applied for hybrid expansion and group of them will assisted by Micro-osteo perforation (MOPs)

control groupintervention group

Eligibility Criteria

Age17 Years - 23 Years
Sexall
Healthy VolunteersNo
Age GroupsChild (0-17), Adult (18-64)
Sampling MethodProbability Sample
Study Population

randamly selected

You may qualify if:

  • An age range from 17-23 years.
  • Transverse maxillary deficiency.
  • Maxillary lingual Cross bite (unilateral or bilateral)
  • No history of previous orthodontic treatment.
  • Good oral and general health.
  • No systemic condition that could interfere with orthodontic treatment.

You may not qualify if:

  • Patient with craniofacial anomalies .
  • History of extraction of permanent teeth.
  • Previous orthodontic treatment.
  • Poor oral hygiene or periodontally compromised patient.
  • Previous history of bruxism, trauma or par functions.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Dental Medicine Al-Azhar University

Cairo, Naser City, 4450113, Egypt

Location

Related Publications (2)

  • Baccetti T, Franchi L, Cameron CG, McNamara JA Jr. Treatment timing for rapid maxillary expansion. Angle Orthod. 2001 Oct;71(5):343-50. doi: 10.1043/0003-3219(2001)0712.0.CO;2.

    PMID: 11605867BACKGROUND
  • McNamara JA. Maxillary transverse deficiency. Am J Orthod Dentofacial Orthop. 2000 May;117(5):567-70. doi: 10.1016/s0889-5406(00)70202-2. No abstract available.

    PMID: 10799117BACKGROUND

MeSH Terms

Conditions

Malocclusion

Interventions

morpholinopropane sulfonic acid

Condition Hierarchy (Ancestors)

Tooth DiseasesStomatognathic Diseases

Study Officials

  • Raafat El ghetany Mohamed, professor

    Al-Azhar University

    STUDY DIRECTOR
  • Ahmed Akram El-Awady, Lecturer

    Al-Azhar University

    STUDY DIRECTOR

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Principal Investigator

Study Record Dates

First Submitted

May 19, 2024

First Posted

June 20, 2024

Study Start

October 1, 2024

Primary Completion

June 1, 2025

Study Completion

August 20, 2025

Last Updated

September 8, 2025

Record last verified: 2025-08

Data Sharing

IPD Sharing
Will not share

Locations