Malocclusion, Angle Class I

3

Review clinical trials related to Malocclusion, Angle Class I. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Not yet recruiting

Treatment Outcome of Elastomeric and Nickel-Titanium Separators in Tooth Separation

Patients seeking fixed orthodontic treatment that requires band placement will be enrolled in this study. This trial aims to compare the efficiency of rectangular cross-section nickel-titanium separators with elastomeric separators in creating sufficient interdental space for orthodontic band placement. In addition, the impact of both separator types on pain perception and gingival health during a 3-day placement period will be evaluated. Participants will be allocated to two groups in a split-mouth design. On the experimental side, nickel-titanium separators will be used, while elastomeric separators will be used as the control on the other side. Outcomes will include separation efficacy, pain perception over time, gingival inflammation, analgesic consumption, and separator loss.

Participants needed: 30
Trial details
Age: 16-25Biological sex: AllType: InterventionalSponsor: 3D-AlignersUpdated: May 15, 2026
Eligibility criteria

Class I skeletal and dental malocclusion. [+6]

Patients presenting with restorations or carious lesions on the proximal surface... [+4]

Status: Not yet recruiting

3D Printed Occlusal Splints for Intraoperative Use

A 3D printed intraoperative occlusal splint is a custom-made biocompatible resin guide that allows surgeons properly align a patient's upper and lower dentition during surgery. This alignment further places maxilla and mandible into proper position. An occlusal splint contains outlines maxillary and mandibular dentition allowing the teeth to lock into place with correct alignment. At Johns Hopkins, traditionally hand-made and industry-made 3D printed splints have been used safely. However, prior studies have demonstrated the ability of in-house 3D prints to save time and money compared to industry. In-house models are similarly produced with FDA-clear, biocompatible resin for 3D printing, and maintain equivalent safety for patients compared to industry-made models.

Participants needed: 70
Trial details
Age: 0-80Biological sex: AllType: InterventionalSponsor: Johns Hopkins UniversityUpdated: Apr 13, 2026
Eligibility criteria

Patients of any age who require any orthognathic surgery (including, but not lim...

Patients who are non-English speaking. [+1]

Status: Not yet recruiting

Effect of Different Grafting Material Following Surgically Facilitated Orthodontics Therapy

The purpose of this study is to quantitatively investigate the radiographic changes of alveolar bone, and gingival tissue changes of the mandibular anterior teeth in experimental group A receiving SFOT using freeze-dried allograft with a collagen membrane, experimental group B receiving SFOT using particulate xenograft covered by a collagen membrane and control group receiving only orthodontics therapy.

Participants needed: 24
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: The University of Texas Health Science Center, HoustonUpdated: Oct 4, 2024Locations: 1
Eligibility criteria

American Society of Anesthesiologists (ASA) I/II [+7]

Patients who are current smokers [+6]