Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
Healthy Volunteers
NCT06502886

Evaluation of The Stability of Orthodontic Treatment After First Premolar Extraction Using Combined Retention Protocol

Led by Cairo University · Updated on 2024-07-16

24

Participants Needed

1

Research Sites

50 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The aim of this study is to compare between the stability of anterior and posterior segments in both arches using bonded lingual retainers versus a combined protocol of retention (bonded lingual retainer and vacuum formed retainers). The effect of different treatment changes achieved on the post-treatment stability will be studied in both groups. Hypothesis: No difference between BR and BR+VFR regarding the stability of anterior segment alignment and posterior segment alignment and interdigitation

CONDITIONS

Official Title

Evaluation of The Stability of Orthodontic Treatment After First Premolar Extraction Using Combined Retention Protocol

Who Can Participate

Age: 18Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Adult patients at the end of comprehensive orthodontic treatment after extraction of upper and lower first premolars and requiring subsequent application of lingual and palatal bonded retainers
  • Good oral hygiene
  • Patients with available pre-treatment records (models)
  • Good finishing criteria according to the ABO grading system
Not Eligible

You will not qualify if you...

  • Orthodontic treatment without extractions
  • Poor oral hygiene
  • Presence of dental or congenital anomalies such as missing laterals, transposed canines, cleft lip and palate, or craniofacial syndromes
  • Poor finishing criteria according to the ABO grading system

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

Faculty of oral and dental medicine, Cairo university

Cairo, Egypt, 11553

Actively Recruiting

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How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

PREVENTION

Number of Arms

2

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