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Effect of MOPs During Orthodontic Movement in Periodontitis Patients (MOPorthoperi)

U

Universidad Complutense de Madrid

Status

Enrolling

Conditions

Orthodontic Tooth Movement
Stage IV Periodontitis

Treatments

Procedure: Micro-ostoperforations (MOPs)

Study type

Interventional

Funder types

Other

Identifiers

NCT06068270
URI_113-210923

Details and patient eligibility

About

Micro-osteoperforations (MOPs) cause cortical bone injuries and consequently increase the expression of inflammatory mediators, allowing for increased bone and periodontal ligament remodeling associated with orthodontic movement. It remains unclear the effect of orthodontic intrusion combined with MOPs application on teeth with reduced periodontium. The general objective will be to determine the efficacy of MOPs during orthodontic tooth movement (OTM) in terms of periodontal and orthodontic outcomes in stage IV periodontitis patients, case type 2 with pathological tooth migration (PTM), characterized the presence of at least one flared tooth of the upper-anterior sextant with an intrabony defect (intrabony component <5mm)

Full description

This is a comparative 2-arm parallel single-blinded randomized controlled clinical trial, with allocation ratio of 1:1, aimed to test an intervention (the use of MOPs) on CAL changes 12 months after placing orthodontic appliances. The control intervention will be the same treatment without the bone traumatic intervention.

Sample: Patients with stage IV periodontitis case type 2 characterized with PTM characterized the presence of at least one flared tooth of the upper-anterior sextant with an intrabony defect (intrabony component <5mm) attending the Post-graduate Program of Periodontology and the Post-graduate Program of Orthodontics of the Faculty of Dentistry at the Complutense University of Madrid (UCM).

Enrollment

28 estimated patients

Sex

All

Ages

18 to 80 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Patients will be included if agreeing to undertake combined periodontal and orthodontic therapy following the clinical practice guideline of stage IV periodontitis patients, and fulfilling the following criteria:

  • adult patients older than 18-year-old;
  • systemically healthy (see exclusion criteria);
  • diagnosed as stage IV (Papapanou et al., 2018) case-type 2 (Herrera et al. 2022) periodontitis;
  • the presence of at least one flared tooth of the upper-anterior sextant with an intrabony defect (intrabonny component <5mm) (experimental teeth);
  • in need of orthodontic therapy.

Exclusion criteria

  • systemic diseases (diabetes mellitus, obesity, cardiovascular diseases);
  • any medication that could affect the level of inflammation, (such as chronic antibiotics, phenytoin, cyclosporin, anti-inflammatory drugs, systemic corticosteroids, or calcium channel blockers);
  • pregnant or lactating woman;
  • inability to respond questions or to attend follow-up visits;
  • extreme skeletal malocclusions requiring orthognathic surgery;
  • patients smoking more than 10 cigarettes/day; and
  • the presence of PD greater or equal to 5mm with BOP after step 3 of periodontal therapy

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

28 participants in 2 patient groups

Test group
Experimental group
Description:
According to randomization, test group patients will receive MOPs at the beginning of the orthodontic therapy and at every other orthodontic recall appointment.
Treatment:
Procedure: Micro-ostoperforations (MOPs)
Control group
No Intervention group
Description:
No MOPs performed at any stage of the orthodontic therapy

Trial contacts and locations

1

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Central trial contact

Elena Figuero, Prof; Conchita Martin, Prof

Data sourced from clinicaltrials.gov

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