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New physiotherapy device for mounth opening in patients with Oral Submucous fibrosis

Development of new physiotherapy device and assessment of its effectiveness compared to traditionally used method in treatment of Oral Submucous Fibrosis: A Randomized Controlled Experimental Study. - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/06/068782
Enrollment
100
Registered
2024-06-12
Start date
Unknown
Completion date
Unknown
Last updated
2024-07-22

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

Conditions

Health Condition 1: R688- Other general symptoms and signs

Interventions

Intervention1: Mouth opening device for physiotherapy along with combination medicine: Mouth opening device for physiotherapy designed for OSMF patients which gives opening and stretching exercises. D

Sponsors

Dr Ashish Bodhade
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Kharra chewing with restricted mouth opening. 2. Clinically diagnosed cases of OSMF stage I, II, & III. 3. Patients willing to participate

Exclusion criteria

Exclusion criteria: Patients less than 18 years and more than 75 years. Any malignancy or any debilitating conditions

Design outcomes

Primary

MeasureTime frame
1. Difference in Interincisal mouth opening (Distance between upper and lower incisors) in millimeter taken by vernier calipper at 3 visits will be compared difference will compared. 1. Base line Interincisal mouth opening 2. After 1month visit 3. After 3 months visit.Timepoint: 1. Base line Interincisal mouth opening 2. After 1month visit 3. After 3 months visit at three point time.

Secondary

MeasureTime frame
3. Improvement in burning sensation an ulceration.Timepoint: 1. First at base line 2. After 1month 3. After 3 months

Countries

India

Contacts

Public ContactAshish S Bodhade

Ranjeet Deshmukh Dental College & Research Centre (RDDC & RC)

dive_alka@rediffmail.com9822992622

Outcome results

None listed

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