Actively Recruiting

Phase Not Applicable
Age: 14Years +
All Genders
NCT07307209

"Sliding Jigs vs Retraction Hooks for Maxillary Dentition Distalization Using IZC Miniscrews"

Led by Sana'a University · Updated on 2026-05-13

40

Participants Needed

1

Research Sites

41 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This randomized controlled clinical trial aims to compare the clinical efficacy, efficiency, and biomechanical differences between two methods for total maxillary dentition distalization: (1) the use of a Sliding Jig and (2) the use of Retraction Hooks, both anchored by Infrazygomatic Crest (IZC) miniscrews. The study will assess rates of distalization, anchorage loss, dentoalveolar tipping, patient comfort, and treatment-associated side effects.

CONDITIONS

Official Title

"Sliding Jigs vs Retraction Hooks for Maxillary Dentition Distalization Using IZC Miniscrews"

Who Can Participate

Age: 14Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Adult patients aged 14 years or older
  • Presence of all permanent teeth fully erupted
  • Bilateral Class II molar relationship skeletal malocclusion
  • Moderate crowding in the upper jaw (less than 5 mm) with maxillary protrusion
  • No craniofacial syndromes present
  • Third molars may be excluded
Not Eligible

You will not qualify if you...

  • Patients with transverse dental or skeletal discrepancies
  • Patients requiring tooth extraction treatment except for third molars or unilateral distalization
  • Patients with a vertical growth pattern
  • Patients with periodontal disease
  • Patients who have had previous orthodontic treatment

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Orthodontic department-faculty of dentistry- Sana'a univeristy

Sanaa, Yemen

Actively Recruiting

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Research Team

N

Nagi H Alawdi, MSc

CONTACT

F

Fuad Luft Almutareb, Prf.

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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