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Laser for Oral Mucositis in Pediatric Onco-hematology (LAMPO)

Primary Purpose

Stomatitis

Status
Completed
Phase
Phase 3
Locations
Italy
Study Type
Interventional
Intervention
Laser therapy
Sham therapy
Sponsored by
IRCCS Burlo Garofolo
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Stomatitis focused on measuring Stomatitis, Laser, Children, Chemotherapy, Treatment

Eligibility Criteria

3 Years - 18 Years (Child, Adult)All SexesDoes not accept healthy volunteers

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

Sites / Locations

  • Policlinico Sant'Orsola Malpighi
  • Spedali civili Ospedale dei Bambini
  • Ospedale Pediatrico Microcitemico "Antonio Cao"
  • Azienda Ospedaliera di Padova
  • Azienda Ospedaliero universitaria di Parma
  • Fondazione IRCCS, Policlinico San Matteo
  • A.O.U. Città della Salute e della Scienza di Torino
  • IRCCS Burlo Garofolo

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Sham Comparator

Arm Label

Laser therapy

Sham therapy

Arm Description

Children are allocated to receive Laser therapy

Children are allocated to receive Sham therapy

Outcomes

Primary Outcome Measures

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

Secondary Outcome Measures

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
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
Reduction of pain, age 4-7 years
Reduction of self-reported pain recorded with the Faces Pain Scale-Revised (FPS-R)
Reduction of pain, age 8-18 years
Reduction of self-reported pain recorded with a numeric rating scale
Reduction of pain, age 4-7 years
Reduction of self-reported pain recorded with the Faces Pain Scale-Revised (FPS-R)
Reduction of pain, age 8-18 years
Reduction of self-reported pain recorded with a numeric rating scale
Reduction of pain, age 4-7 years
Reduction of self-reported pain recorded with the Faces Pain Scale-Revised (FPS-R)
Reduction of pain, age 8-18 years
Reduction of self-reported pain recorded with a numeric rating scale
Reduction of need for analgesics
Adverse events

Full Information

First Posted
April 28, 2016
Last Updated
May 2, 2016
Sponsor
IRCCS Burlo Garofolo
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1. Study Identification

Unique Protocol Identification Number
NCT02762019
Brief Title
Laser for Oral Mucositis in Pediatric Onco-hematology
Acronym
LAMPO
Official Title
LAMPO: Multicenter Randomized Double-blind Controlled Trial to Evaluate the Efficacy of Laser Therapy for Treatment of Oral Mucositis Induced by Chemotherapy in Children
Study Type
Interventional

2. Study Status

Record Verification Date
May 2016
Overall Recruitment Status
Completed
Study Start Date
September 2013 (undefined)
Primary Completion Date
October 2015 (Actual)
Study Completion Date
October 2015 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
IRCCS Burlo Garofolo

4. Oversight

Data Monitoring Committee
No

5. Study Description

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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Stomatitis
Keywords
Stomatitis, Laser, Children, Chemotherapy, Treatment

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
101 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Laser therapy
Arm Type
Experimental
Arm Description
Children are allocated to receive Laser therapy
Arm Title
Sham therapy
Arm Type
Sham Comparator
Arm Description
Children are allocated to receive Sham therapy
Intervention Type
Device
Intervention Name(s)
Laser therapy
Intervention Description
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.
Intervention Type
Device
Intervention Name(s)
Sham therapy
Intervention Description
Only the laser pointer movement, without laser activation, during 4 consecutive days, all over the oral cavity.
Primary Outcome Measure Information:
Title
Reduction of the grade of oral mucositis
Description
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
Time Frame
7 days after enrollment
Secondary Outcome Measure Information:
Title
Reduction of the grade of oral mucositis
Description
Reduction of stomatitis' grade (from grade 3 or 4 to a lower grade). The grade of stomatitis is defined using the WHO evaluation scale
Time Frame
3 days after enrollment
Title
Reduction of the grade of oral mucositis
Description
Reduction of stomatitis' grade (from grade 3 or 4 to a lower grade). The grade of stomatitis is defined using the WHO evaluation scale
Time Frame
11 days after enrollment
Title
Reduction of pain, age 4-7 years
Description
Reduction of self-reported pain recorded with the Faces Pain Scale-Revised (FPS-R)
Time Frame
3 days after enrollment
Title
Reduction of pain, age 8-18 years
Description
Reduction of self-reported pain recorded with a numeric rating scale
Time Frame
3 days after enrollment
Title
Reduction of pain, age 4-7 years
Description
Reduction of self-reported pain recorded with the Faces Pain Scale-Revised (FPS-R)
Time Frame
7 days after enrollment
Title
Reduction of pain, age 8-18 years
Description
Reduction of self-reported pain recorded with a numeric rating scale
Time Frame
7 days after enrollment
Title
Reduction of pain, age 4-7 years
Description
Reduction of self-reported pain recorded with the Faces Pain Scale-Revised (FPS-R)
Time Frame
11 days after enrollment
Title
Reduction of pain, age 8-18 years
Description
Reduction of self-reported pain recorded with a numeric rating scale
Time Frame
11 days after enrollment
Title
Reduction of need for analgesics
Time Frame
at day 7
Title
Adverse events
Time Frame
at day 11

10. Eligibility

Sex
All
Minimum Age & Unit of Time
3 Years
Maximum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
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
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Giulio Andrea Zanazzo, MD
Organizational Affiliation
IRCCS Burlo Garofolo, Trieste
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Matteo Biasotto, DDS
Organizational Affiliation
Azienda Ospedaliero Universitaria "Ospedali Riuniti", Trieste
Official's Role
Study Chair
Facility Information:
Facility Name
Policlinico Sant'Orsola Malpighi
City
Bologna
Country
Italy
Facility Name
Spedali civili Ospedale dei Bambini
City
Brescia
Country
Italy
Facility Name
Ospedale Pediatrico Microcitemico "Antonio Cao"
City
Cagliari
Country
Italy
Facility Name
Azienda Ospedaliera di Padova
City
Padova
Country
Italy
Facility Name
Azienda Ospedaliero universitaria di Parma
City
Parma
Country
Italy
Facility Name
Fondazione IRCCS, Policlinico San Matteo
City
Pavia
Country
Italy
Facility Name
A.O.U. Città della Salute e della Scienza di Torino
City
Torino
Country
Italy
Facility Name
IRCCS Burlo Garofolo
City
Trieste
Country
Italy

12. IPD Sharing Statement

Plan to Share IPD
Undecided

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Laser for Oral Mucositis in Pediatric Onco-hematology

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