ClinicalTrials.Veeva

Menu

Effectiveness of Elastic Chains Versus Elastics in Maxillary Canine Retraction (CREST)

S

Sana'a University

Status

Completed

Conditions

Elastics
Elastic Chains

Treatments

Procedure: Elastics
Procedure: Elastomeric chain

Study type

Interventional

Funder types

Other

Identifiers

NCT07141836
Asraa-H-Ortho

Details and patient eligibility

About

This clinical study aimed to evaluate the effectiveness of Elastics and Elastic chains in maxillary canine retraction. Participants of this study were patients undergoing maxillary canine retraction after first premolar extraction. The study aimed to determine an effective method for better controlling tooth movement.

This study was initiated on 01-2024. Initially, I was not aware of the importance of early registration on ClinicalTrials.gov. Registration was completed after the study began to ensure transparency and adherence to ethical guidelines. All study procedures and protocols have been conducted under the supervision of the academic advisor. All study procedures and protocols have been followed according to institutional and ethical guidelines

Full description

This split-mouth Randomized clinical trial was conducted on 33 patients who needed maxillary canine retraction. Participants were randomly selected one side to receive an elastic chain and the other for elastics, as a method for canine retraction. The intervention period lasted for 15 weeks, and the elastics were replaced by the patient every three days, while elastic chains were exchanged by the principal investigator at 5-week appointments. The type of movement that occurred with each method was evaluated to measure the rate of tooth movement, tipping, and rotation resulting. The study was conducted under the supervision and approval of the Research Ethics Committee at Sana'a University, Faculty of Dentistry. All procedures were performed according to the approved protocol, ensuring participant safety and data accuracy.

Enrollment

33 patients

Sex

All

Ages

14 to 25 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients' treatment required 1st premolar extractions in the maxillary arch and space closure involving canine retraction.
  • Teeth in the buccal segments were without any gross anatomic root anomalies as determined by panoramic radiographs.
  • There is no gross evidence of asymmetric bone loss in the buccal segments of a given arch as determined by panoramic radiographs.
  • Crown/root ratios of contralateral canines and premolars are within 3 mm of one another as determined by panoramic radiographs.

Exclusion criteria

  • Patients with gross anatomical anomalies in upper maxillary canines
  • Patients with growth and development problems.
  • Evidence of bone loss.
  • Presence of Impacted Canine.
  • History of long-term use of NSAIDs and corticosteroids or drugs affect bone metabolism. Patients who reported any medication interfering with bone metabolism or patients with severe skeletal discrepancies indicated for orthognathic treatment.
  • Patients with latex materials allergy.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Crossover Assignment

Masking

Single Blind

33 participants in 2 patient groups

Elastic chains
Experimental group
Description:
This side received maxillary canine retraction using elastic chains
Treatment:
Procedure: Elastomeric chain
Elastics
Experimental group
Description:
This side received maxillary canine retraction with Elastics on the contralateral side of the arch
Treatment:
Procedure: Elastics

Trial documents
1

Trial contacts and locations

1

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems