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Comparing Two Laser Treatments to Reduce Mouth Pain and Sores in Children with Cancer

Comparison of clinical grade, Pain perception and analgesic Use between single and dual Wavelength laser Photobiomodulation in Children with oral mucositis Secondary to cancer therapy: a Randomized controlled trial - nil

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/05/109923
Enrollment
30
Registered
2026-05-04
Start date
Unknown
Completion date
Unknown
Last updated
2026-06-01

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

Conditions

Health Condition 1: K123- Oral mucositis (ulcerative)

Interventions

Intervention1: Combined 660nm plus 810nm dual wavelength laser photobiomodulation: Diode laser (NovoLase Therapy pod, NovoLase Technologies, New Hampshire, USA), combined 660nm and 810nm wavelengths,

Sponsors

Srinivasaragahavan N
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Children aged 3 to 15 years Oral mucositis WHO Grade 2 or greater secondary to cancer therapy Consenting parent and child willing to undergo laser photobiomodulation for 4 consecutive days and return for evaluation on day 7 post enrolment

Exclusion criteria

Exclusion criteria: Previous treatment with photobiomodulation for oral mucositis Presence of dysplastic oral lesions Reduction of mouth opening less than 1 cm Patients undergoing treatment with keratinocyte growth factor Parents and children who refuse the procedure

Design outcomes

Primary

MeasureTime frame
Clinical grade of oral mucositis using WHO Oral Mucositis ScaleTimepoint: Baseline (day 0), day 1, day 2, day 3, day 4 and day 7 post enrolment

Secondary

MeasureTime frame
Pain perception assessed by ChMIESTimepoint: Baseline (day 0), day 1, day 2, day 3, day 4 and day 7 post enrolment;Functional difficulty swallowing, eating, drinking assessed by ChMIESTimepoint: Baseline (day 0), day 1, day 2, day 3, day 4 and day 7 post enrolment;Analgesic use assessed by ChMIESTimepoint: Baseline (day 0), day 1, day 2, day 3, day 4 and day 7 post enrolment

Countries

India

Contacts

Public ContactSRINIVASARAGAHAVAN N

bapuji dental college and hospital

srinijuly2000@gmail.com7299971696

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Jun 11, 2026