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A Comparative Study Between Modified Miniscrew-Assisted Rapid Palatal Expander And Modified Rapid Palatal Expander in Molar Distalization Using Cone- Beam Computed Tomography

A Comparative Study Between Modified Miniscrew-Assisted Rapid Palatal Expander And Modified Rapid Palatal Expander in Molar Distalization Using Cone- Beam Computed Tomography

Status
Active, not recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07038902
Acronym
MIDPAC
Enrollment
24
Registered
2025-06-26
Start date
2025-11-01
Completion date
2027-12-01
Last updated
2025-12-24

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

Conditions

Crowding, Malocclusion, Class I/II, Maxillary First Molar Distalization

Keywords

Modified MARPE, Modified RPE, Molar Distalization, CBCT, Orthodontics

Brief summary

Comparative study between modified miniscrew-assisted rapid palatal expander and modified rapid palatal expander in molar distalization using CBCT.

Detailed description

This research will be conducted as a prospective and randomized clinical trial.

Interventions

DEVICEGroup A: Modified Miniscrew-Assisted Rapid Palatal Expander (MARPE)

A skeletal anchorage-supported with miniscrews inserted into the palate using a self-drilling technique.

DEVICEGroup B: Modified Rapid Palatal Expander (RPE)

A tooth-borne anchorage focusing on molar distalization .

Sponsors

Al-Azhar University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Healthy volunteers
Yes

Inclusion criteria

* Presence of permanent dentition * Skeletal Class I * Dental Class II molar relationship with moderate dental crowding * Crowding \>4mm * Good oral hygiene * Healthy periodontal condition

Exclusion criteria

* Presence of craniofacial syndromes or cleft palate * History of previous orthodontic treatment * Poor oral hygiene or active periodontal disease * Contraindications to CBCT imaging (e.g., pregnancy, inability to remain still during the scan)

Design outcomes

Primary

MeasureTime frame
Amount of Molar Distalization Measured by CBCTBaseline (prior to initiation of molar distalization) At the end of the molar distalization phase (approximately 12 weeks post-treatment initiation).

Countries

Egypt

Outcome results

None listed

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