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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05757024
Other study ID # P.T.REC/012004161
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date August 2, 2022
Est. completion date May 31, 2023

Study information

Verified date February 2023
Source Cairo University
Contact Amira Hassan AbdelTwab, bachelor
Phone 01015598395
Email amirapt21594@gmail.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

this study Randomized controlled study will be conducted to study (the effect of high power laser therapy on radiotherapy induced trismus in head and neck cancer patients). the study group will receive high power laser therapy in combination with conventional tempromandibular joint exercises. the control group will receive conventional tempromandibular joint exercises.


Recruitment information / eligibility

Status Recruiting
Enrollment 44
Est. completion date May 31, 2023
Est. primary completion date April 30, 2023
Accepts healthy volunteers No
Gender All
Age group 20 Years to 65 Years
Eligibility Inclusion Criteria: - head and neck cancer patients who complain of decreased mouth opening and received or receiving radiotherapy. - patients who complain from pain and inflammation in the tempromandibular joint due to radiotherapy. - radiotherapy should be above 40 GY. - patient ages between 20 to 65 years old. Exclusion Criteria: - patients with poor general health. - patients with difficulties in filling questionnaire. - patients who are complaining of other tempomandibular problems other than trismus such as (disc discplacement and trumatic mandibular fractures.

Study Design


Related Conditions & MeSH terms


Intervention

Device:
high power laser therapy
m6 laser therapy of ASA company with multilocked wave system and synchronized emission wave lengths 808 and 905 wave lengths

Locations

Country Name City State
Egypt Faculty of Physical Therapy Cairo University Cairo

Sponsors (1)

Lead Sponsor Collaborator
Cairo University

Country where clinical trial is conducted

Egypt, 

References & Publications (2)

Borges, Marcela Maria Fontes, et al.

Zecha JA, Raber-Durlacher JE, Nair RG, Epstein JB, Elad S, Hamblin MR, Barasch A, Migliorati CA, Milstein DM, Genot MT, Lansaat L, van der Brink R, Arnabat-Dominguez J, van der Molen L, Jacobi I, van Diessen J, de Lange J, Smeele LE, Schubert MM, Bensadou — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary pain level visual analogue scale one month (4 weeks)
Primary mouth opening verneir caliper one month (4 weeks)
Secondary quality of life improvement Washington quality of life questionnaire one month (4 weeks)
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