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Trigger point release on temporomandibular dysfunction by ischemic compression therapy and shock wave therapy.

Analgesic effect of ischemic compression therapy and shock wave therapy for trigger point release on temporomandibular dysfunction.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20240120060742N1
Enrollment
45
Registered
2024-02-15
Start date
2024-03-18
Completion date
Unknown
Last updated
2025-07-21

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

Conditions

Patients who will have experience orofascial pain, pain in the muscles of mastication due to trigger points on the temporomandibular joint will include in this study.. Temporomandibular joint-pain-dysfunction syndrome

Interventions

Intervention 1: Interventional Group 1 will receive ischemic compression therapy. *Baseline treatment was relaxation exercise. *Fist of all patients were relaxation on treatment bed in supine line po

Sponsors

The University of Faisalabad.
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 60 Years

Inclusion criteria

Inclusion criteria: Gender both male and female. Patient age ranges from 20 to 60 year. Patients suffer from painful functional disorder within the masticatory muscles of myofascial characteristics. Chief complaint of acute pain in the joint on at least one side (duration less than 6months). Presence of joint clicking during opening that was eliminated on protrusive opening.

Exclusion criteria

Exclusion criteria: If individual have diabetes, cardiovascular problem, sensory deficient, skin lesion in thearea of trigger point, fibromyalgia and tuberculosis Pregnant women, history of fascial trauma, fracture of facial bone and facial palsy Presence of systemic disease and history of recent trauma

Design outcomes

Primary

MeasureTime frame
Visual analogous scale. Timepoint: At the time of enrollment, later after 3rd and last after the 6th session. Method of measurement: 1-10 Points on paper.;Visual analogous scale. Timepoint: At the time of enrollment, later after 3rd and last after the 6th session. Method of measurement: 1-10 Points on paper.

Secondary

MeasureTime frame
Temporomandibular dysfunction questionnaire before and after treatment. Timepoint: At the time of enrollment, later after 3rd and last after the 6th session. Method of measurement: Questionnaire.

Countries

Pakistan

Contacts

Public Contactkinza Ihsan

University of Faisalabad

dr.kinzaimran95@gmail.com+92 333 7653094

Outcome results

None listed

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