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"Comparing Laser and Ultrasound Therapy for Jaw Joint Pain: A Clinical Study"

Comparative evaluation of Low-Level laser therapy and Therapeutic Ultrasound in the treatment of Temporomandibular joint disorders-A NonRandomised Clinical Trial - nil

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/05/087583
Enrollment
38
Registered
2025-05-26
Start date
Unknown
Completion date
Unknown
Last updated
2026-03-30

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

Conditions

Health Condition 1: M248- Other specific joint derangements,not elsewhere classified

Interventions

Intervention1: Low-Level Laser Therapy: Parameter for laser Laser output-Infrared laser 120mW Wavelength-808 nm Mode and operation continuous Pulse frequency-700-1000Hz Treatment time -2 minutes per

Sponsors

Chettinad Dental College and Research Institute
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1)Participants will be screened and diagnosed with RDC/TMD axis 1 criteria, (the participants of the study will be included with following condition; muscle disorder (MD), disc displacement with reduction (DDR), and disc displacement with reduction associated with muscle disorder (DDR + MD).) 2)Participant age ranges between 18 and 40, 3)Participants willing to take part in this study.

Exclusion criteria

Exclusion criteria: 1) Current or prior orthodontic treatment, under Other treatment for TMD. 2) Current use of analgesic ,anti-inflammatory and psychiatric drug, muscle relaxant 3) A significant malocclusion 4) Absence of more than one tooth per quadrant. 5) Pregnancy and lactating mothers, systemic inflammatory joint disease , arthritis or history of condylar trauma in TMJ within the 4 months before treatment, congenital disturbances as hyperplasia or hypoplasia of joint. 6) Pain associated to odontogenic or neurogenic origin 7) Previous or current history of benign and malignant conditions of TMJ 8) Patients with signs and symptom of other orofacial illness 9) Patient with loss of normal TMJ disc architecture. 10) History of head and neck chemo and radiotherapy. 11) Those who are not willing to participate in this study.

Design outcomes

Primary

MeasureTime frame
Pre and Post evaluation of Muscle Tenderness with Numerical Pain Rating Scale (NPRS)Timepoint: at 0 day,10th day, 1 month

Secondary

MeasureTime frame
Pre and post assessment of functionality of TMDs with Mandibular Functional Impairment QuestionnaireTimepoint: at 0 day,10th day, 1 month

Countries

India

Contacts

Public ContactChamundeeswari P

Chettinad Dental College and Research Institute

christeffimabelr@yahoo.co.in8903777499

Outcome results

None listed

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