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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.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Laser therapy | Experimental | Children are allocated to receive Laser therapy |
|
| Sham therapy | Sham Comparator | Children are allocated to receive Sham therapy |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Laser therapy | Device | Treatment with K-Laser Cube3 during 4 consecutive days, with the following protocol: 660-970 nm wavelength, 3,2W mean power (6.4W pulsating at 50%), 3'51'' duration, 1-20000 Hz frequency, and 1 cm2 spot size. Laser application was performed all over the oral cavity. |
| Measure | Description | Time Frame |
|---|---|---|
| Reduction of the grade of oral mucositis | 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 | 7 days after enrollment |
| Measure | Description | Time Frame |
|---|---|---|
| Reduction of the grade of oral mucositis | Reduction of stomatitis' grade (from grade 3 or 4 to a lower grade). The grade of stomatitis is defined using the WHO evaluation scale | 3 days after enrollment |
| Reduction of the grade of oral mucositis |
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Inclusion Criteria:
Exclusion Criteria:
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| Name | Affiliation | Role |
|---|---|---|
| Giulio Andrea Zanazzo, MD | IRCCS Burlo Garofolo, Trieste | Study Chair |
| Matteo Biasotto, DDS | Azienda Ospedaliero Universitaria "Ospedali Riuniti", Trieste | Study Chair |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Policlinico Sant'Orsola Malpighi | Bologna | Italy | ||||
| Spedali civili Ospedale dei Bambini |
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| ID | Term |
|---|---|
| D013280 | Stomatitis |
| ID | Term |
|---|---|
| D009059 | Mouth Diseases |
| D009057 | Stomatognathic Diseases |
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| ID | Term |
|---|---|
| D053685 | Laser Therapy |
| ID | Term |
|---|---|
| D013812 | Therapeutics |
| D055011 | Ablation Techniques |
| D013514 | Surgical Procedures, Operative |
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|
| Sham therapy | Device | Only the laser pointer movement, without laser activation, during 4 consecutive days, all over the oral cavity. |
|
Reduction of stomatitis' grade (from grade 3 or 4 to a lower grade). The grade of stomatitis is defined using the WHO evaluation scale
| 11 days after enrollment |
| Reduction of pain, age 4-7 years | Reduction of self-reported pain recorded with the Faces Pain Scale-Revised (FPS-R) | 3 days after enrollment |
| Reduction of pain, age 8-18 years | Reduction of self-reported pain recorded with a numeric rating scale | 3 days after enrollment |
| Reduction of pain, age 4-7 years | Reduction of self-reported pain recorded with the Faces Pain Scale-Revised (FPS-R) | 7 days after enrollment |
| Reduction of pain, age 8-18 years | Reduction of self-reported pain recorded with a numeric rating scale | 7 days after enrollment |
| Reduction of pain, age 4-7 years | Reduction of self-reported pain recorded with the Faces Pain Scale-Revised (FPS-R) | 11 days after enrollment |
| Reduction of pain, age 8-18 years | Reduction of self-reported pain recorded with a numeric rating scale | 11 days after enrollment |
| Reduction of need for analgesics | at day 7 |
| Adverse events | at day 11 |
| Brescia |
| Italy |
| Ospedale Pediatrico Microcitemico "Antonio Cao" | Cagliari | Italy |
| Azienda Ospedaliera di Padova | Padova | Italy |
| Azienda Ospedaliero universitaria di Parma | Parma | Italy |
| Fondazione IRCCS, Policlinico San Matteo | Pavia | Italy |
| A.O.U. Città della Salute e della Scienza di Torino | Torino | Italy |
| IRCCS Burlo Garofolo | Trieste | Italy |