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The effect of Photobiomodulation Therapy in the treatment of Radiotherapy-induced Trismus in Head and Neck Cancer patients

The effect of Photobiomodulation Therapy in the treatment of Radiotherapy-induced Trismus in Head and Neck Cancer patients

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-9msvvbq
Enrollment
Unknown
Registered
2022-11-22
Start date
2022-01-02
Completion date
Unknown
Last updated
2025-10-27

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

Conditions

Head and Neck Neoplasms

Interventions

This is a Randomized Clinical Trial, with a sample composed of 27 patients who underwent radiotherapy in the treatment of head and neck cancer and who developed trismus. The patients will be allocated
E02.594.540
E02.594

Sponsors

Irmandade Santa Casa de Misericórdia de Porto Alegre
Lead Sponsor
Irmandade Santa Casa de Misericórdia de Porto Alegre
Collaborator

Eligibility

Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Adult individuals aged 18 years or older, both sexes, in oncologic follow-up for head and neck cancer treatment at Santa Rita Hospital (ISCMPA) who: have undergone radiotherapy treatment for head and neck cancer; have received medical clearance for treatment with photobiomodulation; have a mouth opening equal to or smaller than 35mm.

Exclusion criteria

Exclusion criteria: Individuals with contraindications for the use of photobiomodulation therapy, according to the manufacturer's manual: history of photosensitivity; use of photosensitive medications or cosmetics; undiagnosed clinical lesions; those who exceed 30% of absences throughout the treatment will be excluded; also excluded will be patients who evolve with clinical instability and sensory oscillation that limits adequate understanding regarding the techniques involved in this study.

Design outcomes

Primary

MeasureTime frame
The variable regarding the mouth opening measurement refers to the primary endpoint.

Secondary

MeasureTime frame
The variables related to the AMIOFE score, Visual Analog Scale and quality of life questionnaires are part of the secondary endpoints.

Countries

Brazil

Contacts

Public ContactFelipe Goulart

Irmandade Santa Casa de Misericórdia de Porto Alegre

contato@felipegoulart.com.br+55(51) 3214-8080

Outcome results

None listed

Source: REBEC (via WHO ICTRP)