Skip to content

A study to see if a special physiotherapy and osteopathy program can prevent jaw and facial pain in people after dental treatment

Effectiveness of a PhysiOsteopathic Program to Prevent Temporomandibular and Cervicofacial Pain After Dental Procedures: A Randomized Controlled Trial - NILL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/09/094405
Enrollment
90
Registered
2025-09-08
Start date
Unknown
Completion date
Unknown
Last updated
2025-09-15

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

Conditions

Health Condition 1: M279- Disease of jaws, unspecified

Interventions

Intervention1: PhysiOsteopathic Program: The treatment duration for all intervention arms will follow a structured 4-week protocol. Participants in the cranio cervical physiotherapy and osteopathy gro

Sponsors

Dr Ramesh Chandra Patra
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Participants will be adults aged 18 to 60 years who are scheduled to undergo dental procedures requiring at least 30 minutes of continuous mouth opening. Eligible participants must have no severe or active temporomandibular disorders (TMD) at baseline, as determined by the DC/TMD diagnostic criteria. They must be willing and able to attend physiotherapy sessions following their dental procedure.

Exclusion criteria

Exclusion criteria: Participants will be excluded if they have a history of temporomandibular joint (TMJ) surgery or craniofacial trauma, systemic inflammatory disorders such as rheumatoid arthritis or fibromyalgia, or if they are currently undergoing physiotherapy for TMD or neck pain. Individuals with cognitive or physical impairments that would limit their ability to participate in the study will also be excluded.

Design outcomes

Primary

MeasureTime frame
The primary outcome will be the incidence of clinically significant temporomandibular disorder (TMD) at 3 months following the dental procedure. Clinically significant TMD will be defined as meeting the Diagnostic Criteria for Temporomandibular Disorders (DC/TMD) for pain or dysfunction, accompanied by either a Numeric Rating Scale (NRS) pain score of 3 or higher (on a 0?10 scale) or a Jaw Functional Limitation Scale (JFLS) score of at least 10 points.Timepoint: At baseline,1 week, 4 weeks and 8 weeks

Secondary

MeasureTime frame
The study will assess pain trajectory in the jaw, face, & neck, using the Visual Analog Scale (VAS) or Numeric Rating Scale (NRS). Maximum mouth opening (interincisal distance) & the Jaw Functional Limitation Scale (JFLS-20) will be used to evaluate jaw function, while the Neck Disability Index (NDI) will measure cervical function. Quality of life will be assessed with the Oral Health Impact Profile (OHIP-14) or EQ-5D. Additional parameters include muscle tenderness & trigger point scores, analgesic or rescue medication use, & documentation of any adverse eventsTimepoint: At baseline, 1 week, 4 weeks, & 8 weeks

Countries

India

Contacts

Public ContactDr Ramesh Chandra Patra

Lovely Professional University Faculty of Applied Medical Sciences

ramesh.19500@lpu.co.in09653174563

Outcome results

None listed

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