MedPath

A study to check treatment changes using computerised models in patients with small upper jaw

Phase 1
Registration Number
CTRI/2019/03/017969
Lead Sponsor
Dr Pinky Singh
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Yet Recruiting
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

1) Class III malocclusion with maxillary hypoplasia.

2) Patient giving consent

Exclusion Criteria

1) Unwilling to give consent.

2) Adult and non-growing patient.

3) Patient exhibiting pseudo-class III due to presence of functional shift.

4) Class III skeletal base due to prognathic mandible.

5) Patients with craniofacial syndrome exhibiting maxillary hypoplasia.

6) Patients with craniofacial anomalies, symptoms of TMJ disorders that would require surgical intervention.

7) History of maxillofacial trauma.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Maxillary ProtractionTimepoint: 0,2,8,30,60,90,120,150,180 days post insertion of Facemask and RME.
Secondary Outcome Measures
NameTimeMethod
Increased post protraction stabilityTimepoint: 0,2,8,30,60,90,120,150,180 days post insertion of Facemask and RME.
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