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Clinical Trials/NCT05390320
NCT05390320CompletedNot Applicable

Dental and Periodontal Changes Following the Acceleration of Decrowding of Lower Anterior Teeth Using a PAOO Procedure: A Randomized Controlled Trial

Damascus University1 site in 1 country38 target enrollmentStarted: January 1, 2021Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
38
Locations
1
Primary Endpoint
Change in the inter-canine width

Study Overview

Brief Summary

Patients at the Orthodontic Department of the University of Damascus Dental School will be examined and subjects who meet the inclusion criteria will be included. Then, initial diagnostic records (diagnostic gypsum models, internal and external oral photographs, and radiographic images) will be studied to ensure that the selection criteria are accurately matched.

This study aims to compare two groups of patients with moderate crowding of the lower anterior teeth. Experimental group: the patients in this group will be treated with periodontally accelerated osteogenic orthodontics Control group: the patients in this group will be treated using fixed appliances without any acceleration method.

Detailed Description

Correction of irregular teeth can take a long time, and this depends on various factors such as the good compliance of the patient, the amount of dental crowding, and the need for extraction in the course of orthodontic treatment.

Many methods have been used to accelerate tooth movement, and recently the PAOO technique has emerged as an effective therapeutic intervention.

PAOO is a promising procedure but only a few cases were reported in the literature. Controlled clinical and histological studies are needed to understand the biology of tooth movement with this procedure, the effect on teeth and bone, post-retention stability, measuring the volume of mature bone formation, and determining the status of the periodontium and roots after treatment.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
Single (Outcomes Assessor)

Eligibility Criteria

Ages
18 Years to 28 Years (Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •skeletal class I malocclusion (ANB=2-4)
  • •normal vertical growth pattern.
  • •moderate crowding of lower anterior teeth (i.e., 4-6 millimeters of a tooth size-arch length discrepancy)
  • •1 to 3 mm of overjet and 1 to 4 mm of the overbite
  • •good oral health

Exclusion Criteria

  • •medical, social, and psycho contraindications to oral surgery
  • •presence of periodontal diseases
  • •poor oral hygiene
  • •previous orthodontic treatment

Arms & Interventions

Periodontally accelerated osteogenic orthodontics

Experimental

The patients in this group will be treated by periodontally accelerated osteogenic orthodontics using fixed appliances.

Intervention: PAOO (Procedure)

Conventional treatment

Active Comparator

The patients in this group will be treated using fixed appliances and conventional treatment without any surgical intervention to accelerate tooth movement.

Intervention: Fixed appliance (Other)

Outcomes

Primary Outcomes

Change in the inter-canine width

Time Frame: T0: One day before the beginning of treatment; T1: at the end of the alignment stage

The distance between the cusp tips of the lower canines. This variable will be measured on plaster models.

Change in the inter-2nd premolar width

Time Frame: T0: One day before the beginning of treatment; T1: at the end of the alignment stage

The distance between the central fossae of the lower second premolars. This variable will be measured on plaster models.

Change in Little's Index of Irregularity

Time Frame: T0: one day before the beginning of treatment; T1: after 1 month; T2: after 2 months; T3: after 4 months; T4: after 5 months; T5: at the end of the alignment stage which is expected within 5 - 6 months

The irregularity of the lower incisors is calculated by measuring the amount of deviations of the anatomic contact points between the six anterior teeth in the horizontal direction in mm, since the sum of these measurements represents the value of the index (Little, 1975). The ordinary orthodontic treatment aims to keep this Index less than 1 mm at the end of treatment.

Secondary Outcomes

  • Change in the Plaque index(T0: One day before the beginning of treatment; T1: at the end of the alignment stage)
  • Change in the Papillary Bleeding Index(T0: One day before the beginning of treatment; T1: at the end of the alignment stage)
  • Change in the Gingival index(T0: One day before the beginning of treatment; T1: at the end of the alignment stage)

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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