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N/A N=24 Randomized Single-blind Treatment

A Comparison Between GUMMETAL and SS Orthodontic Wires in Space Closure

Malocclusion, Angle Class I

Enrolled (actual)
24
Serious AEs
0.0%
Results posted
Apr 2024
Primary outcome: Primary: Total Amount of Canine Retraction — 3.41; 3.71 mm

Study Design & Population

Study type
Interventional
Phase
N/A
Interventions
GUMMETAL Orthodontic Wire (Device); Stainless Steel (CrNi) (Device)
Age
Pediatric · 12+ yrs
Sex
All
Sponsor
State University of New York at Buffalo
Primary completion
Mar 2022

Outcome Measures

OutcomeResultp-value
PRIMARY
Total Amount of Canine Retraction
3.41; 3.71
SECONDARY
3-Dimensional Control of Canine Movement Assessment
7.90; 7.25
SECONDARY
Rate of Canine Retraction Per Month
1.14; 1.42

Summary

When there is space present between our teeth orthodontically we have the ability to close them through many methods. Using braces as our treatment modality this study will be investigating how efficient a new orthodontic wire is in closing tooth space. This new material is trade-named GUMMETAL and claims to have many benefits to treating patients orthodontically. We will be exploring its efficiency in space closure compared to an industry standard (stainless steel). We predict that the stainless-steel orthodontic wire will be more efficient at space closure than the new GUMMETAL wires.

Eligibility Criteria

Inclusion Criteria

  • Full permanent dentition (except third molars)
  • Good general and oral health
  • Bilateral spaces 3 >/= mm distal to the maxillary canines
  • Normal and hypodivergent growth pattern
  • Any dental malocclusion
  • Good Oral Hygiene

Exclusion Criteria

  • Systemic diseases or syndrome
  • Abnormalities in teeth size and/or shape
  • Previous orthodontic treatment
  • Anti-inflammatory medication
  • Craniofacial anomalies
  • Hyperdivergent growth pattern
  • Periodontal disease / attachment loss exceeding 25% of root length
  • Significant pre or in-treatment root resorption
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT04591080). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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