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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03287531
Other study ID # 00500
Secondary ID
Status Completed
Phase N/A
First received September 16, 2017
Last updated September 18, 2017
Start date December 10, 2016
Est. completion date August 23, 2017

Study information

Verified date September 2017
Source October 6 University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This study was to determine the effect of conventional therapy and low level laser therapy on pain and function in patients with temporomandibular joint dysfunction. sixty patients with myofascial pain syndrome of TMJ are randomly classified into two groups with thirty patients in each group; Group I received traditional exercise. Group II received low level laser therapy in addition to traditional exercise. All outcome measures including Pain and function, were evaluated before and after the treatment program.


Description:

METHODOLOGY

Subjects: This prospective study was conducted on thirty patients of both genders with myofascial pain syndrome of TMJ in the department of physical therapy at October 6 university Hospital from December 2016 to October 2017. The Patients were selected to be enrolled into this study according to the following criteria:


Recruitment information / eligibility

Status Completed
Enrollment 45
Est. completion date August 23, 2017
Est. primary completion date August 12, 2017
Accepts healthy volunteers No
Gender All
Age group 20 Years to 60 Years
Eligibility Inclusion Criteria:

- All patients are diagnosed as myofascial pain syndrome of TMJ.

Exclusion Criteria:

- Presence of systematic musculo-articular pathologies.

- Pregnant women.

- History of facial trauma.

- Facial palsy.

- Fractures of the facial bones.

Study Design


Related Conditions & MeSH terms


Intervention

Other:
conventional therapy
Exercise therapeutic Ultrasound
low level laser therapy
LLLT with the appropriate parameters (904 nm, 8 j/cm2, 250mw) for duration of 20 min with repletion of three treatment sessions per week.

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Emad Eldin Mohamed

Outcome

Type Measure Description Time frame Safety issue
Primary Pain algometry 4 weeks
Secondary Jaw Functional questionnaire 4 weeks
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