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Completed

NCT Number: NCT03555747

Gingival Crevicular Fluid Cytokine Levels in Response to Orthodontic Forces

The aim of this randomized split-mouth study was to quantify simultaneously 30 analytes including cytokines, chemokines and growth factors in gingival crevicular fluid (GCF) in response to different magnitudes of forces during maxillary canine distalization. The upper right and left canines were distalized using a continuous force of 75 g or 150 g in 15 individuals who had Class II division I malocclusion requiring bilateral extraction of maxillary first premolars. GCF samples were obtained from the tension and the pressure side of each canine at appliance placement and after force application at 24 hours and 28 days. A multiplexed bead immunoassay was used to quantify 30 analytes simultaneously. The effect of force, side and time on the analyte levels were analyzed with Brunner-Langer method.

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Key information

Age range

11 year–16 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

About this study

Patient selection:

Fifteen orthodontic patients with class II division I malocclusion, who required the extractions of maxillary first premolars bilaterally, distal canine movement, and maximum anchorage control as a part of fixed orthodontic treatment plan were invited to participate in the study. All subjects were in good general health with clinically and radiological healthy periodontal tissues (the probing depths ≤3 mm, full-mouth plaque and bleeding score ≤15%, and no bone loss radiographically). Patients were excluded if they were smokers, had had previous orthodontic treatment, had taken a course of anti-inflammatory drugs within 1 month and antimicrobial agents in the previous 3 months prior to the start of the study.

Experimental Design:

The first premolars were extracted at least 20 days prior to the distalization of the canines. Ten days prior to the application of orthodontic force all subjects underwent full-mouth scaling and oral hygiene instructions to ensure optimal plaque control and oral hygiene instruction was reinforced throughout the whole study period. In each patient, two mini-screw implants (1.5 mm in diameter and 8.0 mm in length) were placed bilaterally into the inter-radicular bone between the maxillary second premolar and first molar in the attached gingiva.The upper right and left canines of the same patient were randomly distalized using a continuous force of 75 or 150 g with nickel-titanium closed coil springs. Simple randomization by flipping a coin was used to determine the assignment of each site for two different forces.

GCF sampling:

GCF was sampled from the mesial (tension) and distal (pressure) sides of maxillary right and left canines immediately before appliance placement (baseline) and after force application at 24 hours and 28 days without any reactivation of the coil spring. Baseline measurements of maxillary canines served as a control.

Clinical Periodontal Measurements:

Periodontal clinical parameters including probing depth, clinical attachment loss, gingival index and plaque index were recorded at mesial and distal sites of distally moved canines at baseline and 24 hours and 28 days after force application. All clinical periodontal examinations were performed by a single calibrated periodontist who blinded to the groups using a manual periodontal probe.

Multiplex assay& Quantification of inflammatory mediators:

A commercially available multiplex panel including thirty proteins was used to evaluate GCF content on the Luminex®200 platform.

Determination of the amount of tooth movement:

The distance of maxillary canine movement was measured from the cusp tip of a distally moved canine to the buccal groove of the first permanent molar by using a digital caliper with a sensitivity of ±0.01 mm.

Statistical Analysis:

The data was analysed using a statistical software package. The effect of force, side and time on the analyte levels were analyzed with Brunner-Langer method.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Systemically healthy
  • Non-smoker
  • Orthodontic patients with class II division I malocclusion

Exclusion criteria

  • Orthodontic treatment history
  • Use of anti-inflammatory drugs within one month
  • Use of antibiotics within last three months

Treatment and study plan

Canine distalization

Other

GCF was sampled from the mesial (tension) and distal (pressure) sides of maxillary right and left canines immediately before appliance placement (baseline) and after force application (24 hours and 28 days)

Other names: Gingival crevicular fluid collection

Primary outcomes

  1. Gingival crevicular fluid protein content change

    Time frame: Change from baseline to 24 hours and to 28 days after force application

    pg/ml

Secondary outcomes

  1. Probing pocket depth change

    Time frame: Change from baseline to 24 hours and to 28 days after force application

    mm

  2. Clinical attachment level change

    Time frame: Change from baseline to 24 hours and to 28 days after force application

    mm

  3. The amount of tooth movement

    Time frame: Change from baseline to 28 days after force application

    mm

Sponsors and collaborators

Lead sponsor

Aydin Adnan Menderes University

Other

Collaborators

  • Ege University
  • Karolinska Institutet

Registry information

Official study title

Molecular Analysis of Gingival Crevicular Fluid in Response to the Magnitude of Orthodontic Force: a Longitudinal Randomized Split-mouth Study

Acronym: GCF

Important dates

Study start
2015
Primary completion
2015
Study completion
2015
First posted
Jun 13, 2018
Registry last updated
Jan 14, 2020

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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