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Piezocision-assisted Orthodontic Treatment Combined With Alveolar Bone Regeneration

U

University of Liege

Status and phase

Completed
Phase 4

Conditions

Patients Requiring Mandible Orthodontic Treatment

Treatments

Procedure: Piezocision combined minimally invasive alveolar bone regeneration

Study type

Interventional

Funder types

Other

Identifiers

NCT03655938
P2016-1 In-OP WP2

Details and patient eligibility

About

This study was designed to enroll a series of 10 consecutive patients who met the inclusion criteria. Patients were treated in the Department of Orthodontics and Dento-Facial Orthodopedics of the University of Liège. Two senior's orthodontists and two senior's periodontists were involved in the orthodontic treatment and in the surgical procedures respectively. All clinical, radiographic and periodontal measurements and all orthodontic parameters were performed at baseline and after the orthodontic treatments. Tree examiners collected the overall data.

Enrollment

10 patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion and exclusion criteria

Inclusion criteria:

  • Patients requiring at least mandible orthodontic treatment (both arches)
  • Patient presenting alveolar bone thickness < XX mm
  • Adult patients with completed growth based on the Cervical Vertebral Maturation Method (CVM) as described by Baccetti et al. (Baccetti et al. 2002)
  • Minimal to moderate mandibular anterior crowding at baseline (irregularity index≤6) (Little 1975)
  • American Society of Anesthesiology I or II (I = Normal healthy patient; II = Patients with mild systemic disease)
  • Adequate dento-oral health (i.e., the absence of periodontal diseases, peri-apical infection, or untreated caries).

Exclusion criteria were as follows:

  • Controlled periodontitis with a loss of alveolar support > 10%
  • Gingival recession > 2 mm
  • Smokers
  • Altered bone metabolism (e.g., due to anti-resorptive drug, steroid or immunosuppressant use)
  • Mental or motor disabilities
  • Pregnancy

Trial design

Primary purpose

Prevention

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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