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A Study on the Changes in Patients with Developing Class III Bite Problems Who Were Treated Using a Modified Splint, Class III Elastics, and a Chin Cup Appliance.

Cephalometric and Psychometric evaluation of changes in patients with developing Class III malocclusion treated with the modified Splint Class III Elastics and Chin cup appliance modified sec III an Observational Study - nil

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2025/03/083640
Enrollment
15
Registered
2025-03-28
Start date
Unknown
Completion date
Unknown
Last updated
2025-04-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: K088- Other specified disorders of teethand supporting structures

Interventions

Intervention1: NIL: NIL

Sponsors

MES Dental College and Hospital
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients with developing skeletal Class III malocclusion having bilateral jaw discrepancy or combination of maxillary retrognathism and mandibular prognathism will be included in the study Patients in the age group 10 to 14years Angles Class III malocclusion with Anterior and posterior Crossbite Wit s appraisal of -2.0 mm or less and ANB less than 0 degrees Skeletal maturation CVMI 2 and 3 stage Absence of CO-CR discrepancy (indicating pseudo-Class III malocclusion) Patients should be having healthy gingival and periodontal status

Exclusion criteria

Exclusion criteria: Craniofacial malformations and syndromes Previous orthopedic or orthodontic treatments History of facial trauma Periodontitis History of prolonged treatment with systemic steroids and NSAIDs Systemic diseases including Diabetes mellitus or History of metabolic disorders Presence of cysts tumors and other pathologies Patients with disorders affecting bone healing metabolism and turn over

Design outcomes

Primary

MeasureTime frame
To evaluate and compare the psychological effects using PIDAQ and skeletal dental, soft tissue changes using cephalometric in patients with developing class III malocclusion undergoing modified SEC III protocol at two-time intervals: pre-treatment and post treatmentTimepoint: Before treatment begins typically within a few days or weeks before the intervention starts post treatment after completion of active treatment once the SEC III appliance have concluded—

Secondary

MeasureTime frame
Duration taken for the correction of class III malocclusion by modified SEC III applianceTimepoint: Before treatment begins typically within a few days or weeks before the intervention starts post treatment after completion of active treatment once the SEC III appliance have concluded—

Countries

India

Contacts

Public ContactDr Vincy Antony

Mes dental college

vincyantony2008@yahoo.com9846353153

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026