LAMPO: Multicenter Randomized Double-blind Controlled Trial to Evaluate the Efficacy of Laser Therapy for Treatment of Oral Mucositis Induced by Chemotherapy in Children
Overview
- Phase
- Phase 3
- Intervention
- Not specified
- Conditions
- Stomatitis
- Sponsor
- IRCCS Burlo Garofolo
- Enrollment
- 101
- Locations
- 8
- Primary Endpoint
- Reduction of the grade of oral mucositis
- Status
- Completed
- Last Updated
- 10 years ago
Overview
Brief Summary
Children with cancer undergoing intensive chemotherapy (CT) regimens experience many side effects among which oral mucositis (OM) is one of the most debilitating. Modifications of CT's schedule and prolonged hospitalization may be necessary in presence of OM, causing poor general conditions and debilitation. Moreover, the use of narcotic analgesics and total parenteral nutrition may be required, triggering not only a physical deficit but also an economic burden. Despite the frequency and impact of OM among children with cancer, there is no consensus on standard therapy for this condition. Previous studies demonstrated that high power laser therapy can help the maintenance of nutritional status in patients with OM and can remarkably reduce costs/resources needed. Laser therapy has evidence of efficacy in reducing symptoms and in preventing the onset of OM in adult cancer patients but only one randomized controlled trial, with a limited number of children enrolled, supports its use in children for treatment of OM induced by chemotherapy.
This multicenter double-blind randomized controlled trial evaluates the efficacy of laser for treatment of oral mucositis secondary to chemotherapy in children aged 3-17 years.
The study involves 8 italian hospitals.
Investigators
Ronfani Luca
MD, PhD
IRCCS Burlo Garofolo
Eligibility Criteria
Inclusion Criteria
- •Children aged 3-18 years
- •Oral mucositis of grade 3 or 4 at enrollment (CTC - WHO scale)
- •Antiblastic chemotherapy in the in the previous three weeks
- •Willingness to undergo treatment for 4 consecutive days and to return for evaluation 7 and 11 days after enrollment.
Exclusion Criteria
- •Previous treatment with laser therapy for stomatitis
- •Presence of dysplastic oral lesions
- •Reduction of mouth opening (\<1 cm)
- •Localized head and/or neck radiation treatment in the previous 4 weeks
- •Use of keratinocyte growth factor (KGF)
- •Previous enrollment in the study
Outcomes
Primary Outcomes
Reduction of the grade of oral mucositis
Time Frame: 7 days after enrollment
Reduction of stomatitis' grade (from grade 3 or 4 to a lower grade). The grade of stomatitis is defined using the World Health Organization (WHO) evaluation scale
Secondary Outcomes
- Reduction of pain, age 4-7 years(11 days after enrollment)
- Reduction of need for analgesics(at day 7)
- Reduction of the grade of oral mucositis(11 days after enrollment)
- Reduction of pain, age 8-18 years(11 days after enrollment)
- Adverse events(at day 11)