Actively Recruiting
Effects of Mulligan Mobilization in Comparison With Maitland Mobilization in Temporomandibular Joint Dysfunction.
Led by Foundation University Islamabad · Updated on 2026-01-09
30
Participants Needed
1
Research Sites
17 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
The temporomandibular joint dysfunction is the second most common musculoskeletal pain after back pain, causing jaw pain, restricted movement, and joint sounds. NPRS and millimeter ruler will be used for the assessment of patient. This study will compare the effects of Mulligan and Maitland mobilization, commonly used treatment, on pain and Temporomandibular joint mobility through a randomized controlled trial, involving 30 participants divided into two groups for treatment.
CONDITIONS
Official Title
Effects of Mulligan Mobilization in Comparison With Maitland Mobilization in Temporomandibular Joint Dysfunction.
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age 19 to 44 years
- Male or female gender
- Diagnosed with temporomandibular joint hypomobility using Manual Functional Analysis based on DC/TMD criteria
- Myofascial pain with Numeric Rating Scale score above 5 and pain on palpation in at least two of eight masticatory or neck muscles
- Acute temporomandibular disorder and myofascial pain not related to active inflammation, infection, or recent trauma for at least six months
You will not qualify if you...
- Hypermobility of temporomandibular joints
- Pregnancy
- History of rheumatic or inflammatory diseases
- Treatment for temporomandibular disorders within the last three months
- Acute trauma or injuries to face, head, or cervical spine
- Neurological disorders
- Taking medications that affect the musculoskeletal system
AI-Screening
AI-Powered Screening
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Trial Site Locations
Total: 1 location
1
Foundation University College of Physical Therapy
Islamabad, Punjab Province, Pakistan
Actively Recruiting
Research Team
M
Mah Noor
CONTACT
A
Anam Rehman, MS-OMPT
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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