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Clinical Trials/PACTR202309912835123
PACTR202309912835123
Completed
Phase 4

Comparison of dentofacial and skeletal effects of intermaxillary NiTi coil springs and intermaxillary elastics in the treatment of Class II malocclusion among adolescents.

Dr. Esan Tolulope Bolanle0 sites48 target enrollmentAugust 2, 2023
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ConditionsOral Health

Overview

Phase
Phase 4
Intervention
Not specified
Conditions
Oral Health
Sponsor
Dr. Esan Tolulope Bolanle
Enrollment
48
Status
Completed
Last Updated
2 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
August 2, 2023
End Date
TBD
Last Updated
2 years ago
Study Type
Interventional
Sex
All

Investigators

Sponsor
Dr. Esan Tolulope Bolanle

Eligibility Criteria

Inclusion Criteria

  • •1\. Class II Molar and/or canine relationship with at least half unit cusp disto\-occlusion on one or both sides of the jaw.
  • •2\.Subjects aged 10\-19years old
  • •3\.Presence of all permanent teeth up to first molar
  • •4\.Minimum overjet of 5mm
  • •5\.Subjects with complete pre\-treatment records which are lateral cephalometric radiograph, study models and clinical photographs.
  • •6\.Subjects who have completed the levelling and alignment phase of non\-extraction fixed orthodontic therapy with Roth 0\.022 prescription and are on upper and lower 0\.019x0\.025\-inch Stainless steel wires.
  • •7\.Subjects between 10\-15years must give assent (Appendix 2\) and subject’s parent must give consent. While subjects between 16\-19years must give consent.

Exclusion Criteria

  • •1\. Subjects with syndromic or craniofacial abnormalities such as cleft lip and palate.
  • •2\. Subjects with missing permanent tooth not including second and third molars.
  • •3\. Subjects with missing or incomplete records.
  • •4\. Subjects with springs that showed permanent deformation at any of the recall visits.
  • •5\. Subjects allergic to latex and nickel titanium.
  • •6\. Subjects on routine medications such as contraceptives, bisphosphonates or non\-steroidal anti\-inflammatory drugs (NSAIDs).
  • •7\. Subjects not willing to participate in the study.

Outcomes

Primary Outcomes

Not specified

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