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Randomized Controlled Trial of Orofacial Myofunctional Therapy in Children With Anterior Open Bite and Atypical Swallowing During Early and Intermediate Mixed Dentition

Evaluation of the effect of Orofacial Myofunctional Treatment in children with anterior open bite and atypical swallowing patterns in early and intermediate mixed dentition: A randomized controlled trial - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/06/113172
Enrollment
160
Registered
2026-06-30
Start date
Unknown
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

None listed

Interventions

Intervention1: 1.OMT 2.OMT+ orthodontic treatment: 1.For OMT group:-10 hours of OMT, during 10-20 sessions of 30-60 minutes and exercises at home 2.OMT+ Orthodontic treatment:- 10 hours of OMT,

Sponsors

Dr Gunesh Pande
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Children aged 6-9 years having atypical swallowing pattern and anterior open bite in early and intermediate mixed dentition 2. Children with orofacial myofunctional disorders 3. Children with early or intermediate mixed dentition 4. Children having visceral swallowing pattern 5. Parents/guardian who provide informed consent

Exclusion criteria

Exclusion criteria: 1. Children with age less than 6 or more than 10 years 2. Children with systemic diseases, syndromes 3. Conditions such as cleft lip and palate 4. Children with intellectual disability and craniofacial abnormalities 5. Previous or ongoing orofacial myofunctional therapy 6. Sucking habits not ceased for at least 6 months prior to intake

Design outcomes

Primary

MeasureTime frame
The study is expected to demonstrate that the children in the experimental group receiving Orofacial Myofunctional Treatment will show marked improvements in tongue posture, swallowing biomechanics, and hyoid bone dynamics compared to the control group. Ultrasonography is anticipated to reliably capture these functional changes, validating USG as an objective, child-friendly tool for assessing therapeutic progress.Timepoint: 1 month,3 months and 6 months after the intervention

Secondary

MeasureTime frame
Improvement in occlusal relationship. Increased perioral muscle activity & coordination. Development in specch articulation & oral motor skills. Patient compliance & acceptability of the therapy. Stability of outcomes after 6 month followup. Timepoint: 1month, 3 months , 6 months

Countries

India

Contacts

Public ContactDr Gunesh Pande

Dr. D. Y. Patil Dental College and Hospital

drmadhura4@gmail.com9860079769

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Aug 10, 2026