OC and ICTP in Gingival Crevicular Fluid During Piezocision Accelerated Orthodontic Treatment

Sponsor
Marmara University (Other)
Overall Status
Completed
CT.gov ID
NCT04611984
Collaborator
(none)
15
1
2
17
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Study Details

Study Description

Brief Summary

The aim of this study was to evaluate the tooth movement with and without piezocision with regard to the levels of osteocalcin and cross-linked C-terminal telopeptides of type I collagen in the gingival crevicular fluid.

Condition or Disease Intervention/Treatment Phase
  • Procedure: Piezocision
  • Procedure: Control
N/A

Detailed Description

15 systemically healthy subjects requiring extraction of the maxillary 1. premolars with distalization of the maxillary canines were enrolled to the study. Piezocisions were performed on the distal and mesial sides of the right maxillary canines while the left maxillary canines served as controls. Canine distalization was performed via closed-coil springs applying 150 g of force per side by using miniscrews as anchorage. Gingival crevicular fluid samples were collected from both mesial and distal sides of right and left maxillary canines at 0, 1, 7, 14 and 28 days. The gingival crevicular fluid levels of osteocalcin and cross-linked C-terminal telopeptides of type I collagen were determined by using ELISA. The rate of tooth movement was measured on 14 and 28 days.

Study Design

Study Type:
Interventional
Actual Enrollment :
15 participants
Allocation:
Non-Randomized
Intervention Model:
Crossover Assignment
Masking:
Double (Investigator, Outcomes Assessor)
Masking Description:
The investigators performing the clinical and surgical procedures, and patients were not blinded. Data assessment was performed by a blinded researcher. Gingival crevicular fluid samples were collected and numbered by another blinded researcher.
Primary Purpose:
Treatment
Official Title:
Osteocalcin and Cross-Linked C-Terminal Telopeptides of Type I Collagen in Gingival Crevicular Fluid During Piezocision Accelerated Orthodontic Tooth Movement
Actual Study Start Date :
Mar 1, 2013
Actual Primary Completion Date :
Aug 1, 2014
Actual Study Completion Date :
Aug 1, 2014

Arms and Interventions

Arm Intervention/Treatment
Experimental: Piezocision

Piezocision was performed on the mesial and distal side of the maxillary right canine tooth which was served as the piezocision group. Then canine distalization was performed via closed-coil springs applying 150 g of force by using mini-screws as anchorage.

Procedure: Piezocision
Piezocisions were performed on the mesial and distal sides of the right maxillary canines. Then canine distalization was performed via closed-coil springs applying 150 g of force by using mini-screws as anchorage.

Active Comparator: Control

Maxillary left canine served as the control group and canine distalization was performed via closed-coil springs applying 150 g of force by using mini-screws as anchorage.

Procedure: Control
The mesial and distal sides of the left maxillary canines served as controls and canine distalization was performed via closed-coil springs applying 150 g of force by using mini-screws as anchorage.

Outcome Measures

Primary Outcome Measures

  1. Gingival crevicular fluid osteocalcin level (ng/ml) [28 days after canine distalization]

    Gingival crevicular fluid samples were collected from mesial and distal sides of the maxillary right and left canines.The gingival crevicular fluid level of osteocalcin was determined by using ELISA

  2. Gingival crevicular fluid cross-linked C-terminal telopeptides of type I level (ng/ml) [28 days after canine distalization]

    Gingival crevicular fluid samples were collected from mesial and distal sides of the maxillary right and left canines.The gingival crevicular fluid level of cross-linked C-terminal telopeptides of type I collagen was determined by using ELISA.

Secondary Outcome Measures

  1. The amount of canine movement (mm) [Baseline (day 0) before canine distalization and, 14 and 28 days after canine distalization]

    All measurements were performed on the dental cast model using a digital caliper. The amount of space closure was based on the measurements of the distance between the contact points of the distal surface of canine and the mesial surface of second premolar. The change of distance between the three observation periods represented the amount of canine movement.

  2. Retraction rate (mm/day) of canine movement [14 and 28 days after canine distalization]

    All measurements were performed on the dental cast model using a digital caliper. The amount of space closure was based on the measurements of the distance between the contact points of the distal surface of canine and the mesial surface of second premolar. The change of distance between the three observation periods represented the amount of canine movement, which was divided by the number of days between two sessions to obtain the retraction rate on daily basis

Eligibility Criteria

Criteria

Ages Eligible for Study:
13 Years to 20 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Class I, Class II or Class III malocclusion,

  • Proclined incisors requiring extraction of the maxillary first premolars with subsequent retraction of the maxillary canines

  • No previous orthodontic treatment

  • Good oral hygiene and periodontal health (plaque and gingival indices less or equal 1, probing depth less or equal 3 mm, no radiographic bone loss).

Exclusion Criteria:
  • having systemic diseases that could affect bone and tooth movement

  • smoking

Contacts and Locations

Locations

Site City State Country Postal Code
1 Marmara University Faculty of Dentistry İstanbul Turkey 34854

Sponsors and Collaborators

  • Marmara University

Investigators

  • Principal Investigator: Hatice Selin Yıldırım, Dr., Marmara University, Faculty of Dentistry, Department of Peridontology

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Marmara University
ClinicalTrials.gov Identifier:
NCT04611984
Other Study ID Numbers:
  • 04.03.2013.38
First Posted:
Nov 2, 2020
Last Update Posted:
Nov 2, 2020
Last Verified:
Oct 1, 2020
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Marmara University

Study Results

No Results Posted as of Nov 2, 2020