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NCT Number: NCT06458517

Evaluation of Two Methods of Administration of Photobiomodulation in the Context of the Prevention and Treatment of Mucositis Induced by Radiotherapy, During the Treatment of Head and Neck Cancers

The aim of this feasibility, prospective, single-center trial is to compare an intra-oral Photobiomodulation (PBM) via the Caremin650TM device (NeoMedLight) and a transcutaneous PBM via the ATP 38® device (Swiss Bio Innov) in patients treated with radiotherapy or chemoradiotherapy for cancer of the oropharynx or oral cavity. PBM session will be carried out first at the rate of two sessions per week for preventive purposes, and then, in case of occurence of grade 1 mucositis, three sessions per week with curative purpose.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Institut de cancérologie Strasbourg Europe

Strasbourg, 67033, France

Location contact

Manon VOEGELIN

CONTACT

[email protected]

368339523 ext. +33

About this study

Oral mucositis (OM) is defined as damage to the mucosa of the oral cavity; it can be due to chemotherapy or radiotherapy. The incidence of OM is 59 to 100% according to studies in patients with oral cavity or oropharyngeal cancer receiving radiotherapy.

Clinically, OM is characterized by erythematous changes in the mucosa, which can progress to oral ulcerations. It can significantly alter the quality of life, the ability to eat, cause weight loss in patients and interfere with the proper realization of anti-tumoral treatment. Additionally, OM may increase the risk of bacteremia and sepsis in immunocompromised patients.

So far, effective management strategies for OM and associated pain are still insufficient. A wide variety of topical and oral agents are available, but effectiveness is still lacking.

Photobiomodulation (PBM) therapy involves the application of visible or infrared light produced by laser diodes or light-emitting diodes (LEDs) to stimulate wound healing, reduce inflammation, and decrease pain.

PBM can be performed in two main ways: intraoral and transcutaneous. Intraoral PBM involves applying red or near-infrared light directly in contact with the oral mucosa, while transcutaneous PBM involves the application of infrared radiation to the skin. Both techniques have shown their effectiveness. Numerous trials have evaluated the impact of PBM in radiomucositis but its use in clinical practice is to date not widespread and heterogeneous.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Adult patient (18 years old and older);
  • Patients with oral cavity or oropharynx cancer treated with radiotherapy or chemo-radiotherapy;
  • Karnofsky Performance Status > 60%;
  • Able to understand French;
  • With signed informed consent;
  • Affiliated to French Health Security Insurance

Exclusion criteria

  • Allergy to polyurethanes;
  • Head and Neck tumors that are localized to other sites than oral cavity or oropharynx
  • Previous irradiation of Head and Neck (whatever the time lapse between the two irradiations)
  • Pregnant and breastfeeding woman;
  • Patients with pacemaker device
  • Epileptic patients;
  • Concomitant treatment or treatment within the 7 days before inclusion with one of several drugs from the following list: fluoroquinolones, cycline, methotrexate, auranofin
  • Patients with ophthalmic diseases (such as maculopathy, retinopathy, glaucoma and cataract, retinal damage)
  • Patients under judicial protection

Treatment and study plan

Photobiomodulation session - intraoral

Device

use of CareMin650TM lightbox(NeoMedLight) in preventive and in case of occurence of grade 1 oral mucositis, in curative purpose

Photobiomodulation session - transcutaneous

Device

use of ATP38® phototherapy device (Swiss Bio Inov Europe) in preventive and in case of occurence of grade 1 oral mucositis, in curative purpose

Primary outcomes

  1. Cumulative incidence of oral mucositis (grade ≥ 2) in both group (intraoral and transcutaneous PBM)

    Time frame: Until OM resolution, up to 12 weeks

    Oral mucositis will be graded according to NCI-CTCAE V5.0 criteria

Secondary outcomes

  1. Radiotherapy treatment interruption in both group (intraoral and transcutaneous PBM)

    Time frame: Until OM resolution, up to 12 weeks

    Number of cancelled radiotherapy sessions in comparison to initial treatment plan

  2. Duration of oral mucositis in both group (intraoral and transcutaneous PBM)

    Time frame: Until OM resolution, up to 12 weeks

    Number of days

  3. Number of hospitals stays in both group (intraoral and transcutaneous PBM)

    Time frame: Until OM resolution, up to 12 weeks

    Number of unscheduled hospitalizations

  4. Number of introductions of parenteral nutrition in both group (intraoral and transcutaneous PBM)

    Time frame: Until OM resolution, up to 12 weeks

    Number of days from radiotherapy initiation until artificial nutrition introduction

  5. Infection rate in both group (intraoral and transcutaneous PBM)

    Time frame: Until OM resolution, up to 12 weeks

    Infections graded according to NCI-CTCAE V5.0 criteria

  6. Food intake in both group (intraoral and transcutaneous PBM)

    Time frame: Until OM resolution, up to 12 weeks

    Measured on a weekly basis with the Simple Evaluation of Food Intake (SEFI) tool

  7. Pain level in both group (intraoral and transcutaneous PBM)

    Time frame: Until OM resolution, up to 12 weeks

    Measured with a visual analogic scale (VAS), graded from 0 to 10

  8. Quality of life of patients in both group (intraoral and transcutaneous PBM)

    Time frame: Until OM resolution, up to 12 weeks

    Questionnaire from EORTC: QLQ-C30 with organ specific QLQ-HN35 module

  9. Dry mouth rate in both group (intraoral and transcutaneous PBM)

    Time frame: Until OM resolution, up to 12 weeks

    Graded according to NCI-CTCAE V5.0 criteria

Study contacts

Contact information is provided by the study sponsor or research team.

Manon VOEGELIN

CONTACT

[email protected]

VOEGELIN ext. +33

Sponsors and collaborators

Lead sponsor

Centre Paul Strauss

Other

Registry information

Official study title

Pilot Observational Study of Transcutaneous and Intraoral Photobiomodulation in the Prevention and Treatment of Radiomucositis in Head and Neck Cancers Treated by Radiotherapy - RADIO-PBM Trial

Acronym: RADIO-PBM

Important dates

Study start
2026
Primary completion
2029
Study completion
2029
First posted
Jun 13, 2024
Registry last updated
Jun 5, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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