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Biological Markers Evaluation of Accelerated Tooth Movement

U

University of Sao Paulo

Status

Unknown

Conditions

Cytokine Measurements
Tooth Movement
Orthodontic Space Closure

Treatments

Procedure: micro-osteoperforation

Study type

Interventional

Funder types

Other

Identifiers

NCT02887547
Fattori2

Details and patient eligibility

About

Gingival Crevicular Fluid samples will be collected using periopapers after accelerated tooth movement technique, results will be assessed with biomarkers levels done using ELISA Assays

Full description

For this prospective study, 22 individuals were selected, with skeletal discrepancies randomly divided into two groups: 1 - accelerated tooth movement technique (ATMT) and 2 - Control.

Orthodontic records done in two times, initial and preoperative; Gingival Crevicular Fluid samples will be collected using periopapers in 7 times (1, 2, 7, 14, 28 days and after space closure- end of orthodontic treatment movement activation).

Flapless cortical perforations will be made in ATMT Group after dental extraction. Surgical protocol will be flapless to preserve periodontal health.

After extraction space closure, results will be assessed by clinical effects with biological markers levels:

CCL3/MIP-1 alpha, CCL5/RANTES, CXCL8/IL8, IL-1 alpha, IL-1 beta, IL6, TNF-alpha, TRANCE/RANK L, OCN OPG IL-10 VEGF TGF-ℬ

Those biomarkers levels will be performed using ELISA Assays. After collecting data, the results will be statistically analyzed using Shapiro-Wilk and, posteriorly, T-student or Wilcoxon.

Enrollment

25 patients

Sex

All

Ages

18 to 40 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Adult subjects ages 18-40 years old, in good general health, with adult complete dentition, regardless of presence of third molars.
  • Indication for orthognathic surgery
  • Tooth extraction indication for orthodontic treatment
  • Do not smoke
  • Periodontal and teeth healthy
  • Do not use bisphosphonates or corticosteroids

Exclusion criteria

  • Surgically assisted rapid palatal expansion indication
  • Cleft lip and palate
  • Craniofacial syndrome
  • Mental disorder
  • Metabolic diseases

Trial design

Primary purpose

Diagnostic

Allocation

Randomized

Interventional model

Crossover Assignment

Masking

None (Open label)

25 participants in 2 patient groups

Control
No Intervention group
Description:
Control group, with traditional orthodontic mechanics for anterior retraction. Crevicular fluid will be collected during anterior retraction mechanics to identified biomarkers in the inflammatory process
Acceleration
Experimental group
Description:
Group with micro-osteoperforation for accelerated tooth movement during anterior retraction, Crevicular fluid will be collected during anterior retraction mechanics to identified biomarkers in the inflammatory process
Treatment:
Procedure: micro-osteoperforation

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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