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Cryotherapy for Prevention of Oral Mucositis in Children Undergoing Hematopoietic Stem Cell Transplantation

Primary Purpose

Oral Mucositis, Pain, Infection

Status
Completed
Phase
Not Applicable
Locations
Sweden
Study Type
Interventional
Intervention
Cryotherapy
Sponsored by
Uppsala University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Oral Mucositis focused on measuring Oral Mucositis, Children, Cryotherapy, Hematopoietic Stem Cell Transplantation

Eligibility Criteria

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

Inclusion Criteria:

Age between 4-18 Undergoing Hematopoietic Stem Cell Transplantation in Sweden sufficient knowledge in swedish to understand the protocols -

Exclusion Criteria:

-

Sites / Locations

  • Pediatric Oncology Department, Queen Silvia Childrens´ Hospital
  • Departent of Pediatric Oncology, Lund University Hospital
  • Center for Allogeneic Stem Cell Transplantation, Karolinska University Hospital, Hudding
  • Department of pediatrics B78, Karolinska University Hospital
  • Department of Hematology, Uppsala University Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

Cryotherapy

Control

Arm Description

Cryotherapy during conditioning treatment with chemotherapy prior to HSCT

Standard oral Care. No Cryotherapy during conditioning treatment prior to HSCT

Outcomes

Primary Outcome Measures

Mucositis grade - WHO Oral Toxicity Scale
WHO-Oral toxicity scale Grade 0 - No mucositis Grade 1 - Erythema and/or soreness Grade 2 - Erythema and/or ulcers. Can eat solid food. Grade 3 - Erythema and/or Ulcers. No solid food but can ingest liquids. Grade 4 - Oral alimentation not possible.

Secondary Outcome Measures

Mucositis grade - Children´s International Mucositis Evaluation Scale (ChiMES)
Daily evaluation by child and parent.
Pain - Childrens Hospital Eastern Ontario Pain Scale (CHEOPS)
Daily assessment by nurse
Mouth Pain
Mouth Pain measured with Numerical Rating scale(NRS)for children >7 years and parents and Facial Pain Scale(FPS) for children < 7 years
Emotional and Psychological status
Beck youth inventories for depression and anxiety

Full Information

First Posted
February 5, 2013
Last Updated
October 26, 2016
Sponsor
Uppsala University
Collaborators
The Swedish Childhood Cancer Foundation
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1. Study Identification

Unique Protocol Identification Number
NCT01789658
Brief Title
Cryotherapy for Prevention of Oral Mucositis in Children Undergoing Hematopoietic Stem Cell Transplantation
Official Title
A Randomized Controlled Trial of Cryotherapy for Prevention and Reduction of Severity of Oral Mucositis in Children Undergoing Hematopoietic Stem Cell Transplantation.
Study Type
Interventional

2. Study Status

Record Verification Date
October 2016
Overall Recruitment Status
Completed
Study Start Date
October 2012 (undefined)
Primary Completion Date
June 2016 (Actual)
Study Completion Date
October 2016 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Uppsala University
Collaborators
The Swedish Childhood Cancer Foundation

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Oral mucositis (OM) is a common adverse effect of chemotherapy, radiotherapy and conditioning regimens before Hematopoietic Stem Cell Transplantation (HSCT). The aim of this study is to effectiveness of cryotherapy as a prophylactic treatment in children undergoing HSCT.
Detailed Description
There is a complex pathobiology behind OM; chemo and radiotherapy affects the mucosa and submucosa causing DNA-strand brakes and generation of reactive oxygen species (ROS). This initiates a cascade of events, among others activation of transcription factors, up-regulation of pro-inflammatory cytokines, and activation of macrophages and proteases leading to tissue injury causing symptoms such as erythema, edema, ulceration, taste perception alterations, and mouth dryness. OM often causes local and systemic infections, fatigue, pain, and difficulties in basal functions such as swallowing (and hence drinking and eating) and talking and reduces patients' psychological well-being. Nearly 90 % of pediatric patients undergoing HSCT are afflicted with OM. In pediatric patients mucositis is reported as one of the most painful and debilitating side effects during cancer treatment.Beyond a significant suffering for the patient it is hence associated with higher costs for health care and increased mortality. The current scientific situation regarding prevention and treatment of OM has been summarized in Cochrane reports showing limited data on adults and practically missing data on children and adolescents. Concluding guidelines from these reports emphasize the need for well conducted randomized controlled trials (RCT's) to evaluate and refine treatments in order to establish evidence based interventions. The use of cryotherapy to prevent oral mucositis in patients who are receiving high-dose chemotherapy as a conditioning agent prior to HSCT continue to show evidence in the adult population. The aim of this study is to compare treatment with cryotherapy (Arm 1)with a standard oral care protocal (Arm 2) ARM 1 Children are instructed to use chew on ice-chips, ingest ice-cream or ice-water during infusion of chemotherapy as part of the conditioning treatment prior to HSCT. Melted ice should be replaced by new as soon as possible. Children receiving a 24-hour infusion are instructed to use cryotherapy for one hour 4 times a day. ARM 2 Standard care for prevention and management of oral mucositis Primary outcome Degree and duration of Oral mucositis Secondary outcomes Oral pain Opioid use Duration of parenteral nutrition Weight loss Duration of neutropenic fever Duration of antibiotic treatment Duration of hospitalization Emotional and psychological status C reactive protein (CRP) and s-albumin correlation to grade of Oral Mucositis

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Oral Mucositis, Pain, Infection, Nutrition Aspect of Cancer
Keywords
Oral Mucositis, Children, Cryotherapy, Hematopoietic Stem Cell Transplantation

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Investigator
Allocation
Randomized
Enrollment
53 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Cryotherapy
Arm Type
Experimental
Arm Description
Cryotherapy during conditioning treatment with chemotherapy prior to HSCT
Arm Title
Control
Arm Type
No Intervention
Arm Description
Standard oral Care. No Cryotherapy during conditioning treatment prior to HSCT
Intervention Type
Other
Intervention Name(s)
Cryotherapy
Intervention Description
Cryotherapy with ice-chips, ice cream or ice water is given during conditioning treatment with chemotherapy prior to HSCT.
Primary Outcome Measure Information:
Title
Mucositis grade - WHO Oral Toxicity Scale
Description
WHO-Oral toxicity scale Grade 0 - No mucositis Grade 1 - Erythema and/or soreness Grade 2 - Erythema and/or ulcers. Can eat solid food. Grade 3 - Erythema and/or Ulcers. No solid food but can ingest liquids. Grade 4 - Oral alimentation not possible.
Time Frame
Daily until engraftment, an expected average of 20 days.
Secondary Outcome Measure Information:
Title
Mucositis grade - Children´s International Mucositis Evaluation Scale (ChiMES)
Description
Daily evaluation by child and parent.
Time Frame
Daily until engraftment, an expected average of 20 days.
Title
Pain - Childrens Hospital Eastern Ontario Pain Scale (CHEOPS)
Description
Daily assessment by nurse
Time Frame
Daily until Engraftment an expected average of 20 days.
Title
Mouth Pain
Description
Mouth Pain measured with Numerical Rating scale(NRS)for children >7 years and parents and Facial Pain Scale(FPS) for children < 7 years
Time Frame
Daily until Engraftment an expected average of 20 days
Title
Emotional and Psychological status
Description
Beck youth inventories for depression and anxiety
Time Frame
Daily until engraftment, an expected average of 20 days.
Other Pre-specified Outcome Measures:
Title
Opioid consumption
Description
Days with, and dose of morphine-equivalent opioids
Time Frame
During hospitalization in connection with HSCT, an expected average of 25 days
Title
Duration of parenteral nutrition
Description
Days with Total Parenteral Nutrition
Time Frame
During hospitalization in connection with HSCT, an expected average of 25 days
Title
Weight Loss
Description
Weight Loss in kilograms from admission to date of engraftment
Time Frame
During hospitalization in connection with HSCT, an expected average of 25 days
Title
Duration of Antibiotic treatment
Description
Days with antibiotics
Time Frame
During hospitalization in connection with HSCT, an expected average of 25 days
Title
Duration of febrile neutropenia
Description
Days with fever >38.0 degrees
Time Frame
Until engraftment, an expected average of 20 days
Title
Duration of Hospitalisation
Description
Counted from day 0 until discharge either home or to region hospital.
Time Frame
During hospitalization in connection with HSCT, an expected average of 25 days
Title
C reactive protein
Description
Level of p-CRP in comparison to grade of mucositis
Time Frame
During hospitalization in connection with HSCT, an expected average of 25 days
Title
S-Albumin
Description
In correlation to grade of Oral Mucositis
Time Frame
During hospitalization in connection with HSCT, an expected average of 25 days

10. Eligibility

Sex
All
Minimum Age & Unit of Time
4 Years
Maximum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age between 4-18 Undergoing Hematopoietic Stem Cell Transplantation in Sweden sufficient knowledge in swedish to understand the protocols - Exclusion Criteria: -
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Gustaf Ljungman, MD, PhD
Organizational Affiliation
Uppsala University
Official's Role
Study Director
Facility Information:
Facility Name
Pediatric Oncology Department, Queen Silvia Childrens´ Hospital
City
Gothenburg
ZIP/Postal Code
SE-41685
Country
Sweden
Facility Name
Departent of Pediatric Oncology, Lund University Hospital
City
Lund
ZIP/Postal Code
SE-22185
Country
Sweden
Facility Name
Center for Allogeneic Stem Cell Transplantation, Karolinska University Hospital, Hudding
City
Stockholm
ZIP/Postal Code
SE-14186
Country
Sweden
Facility Name
Department of pediatrics B78, Karolinska University Hospital
City
Stockholm
ZIP/Postal Code
Se-14186
Country
Sweden
Facility Name
Department of Hematology, Uppsala University Hospital
City
Uppsala
ZIP/Postal Code
SE-75185
Country
Sweden

12. IPD Sharing Statement

Citations:
PubMed Identifier
31993753
Citation
Kamsvag T, Svanberg A, Legert KG, Arvidson J, von Essen L, Mellgren K, Toporski J, Winiarski J, Ljungman G. Prevention of oral mucositis with cryotherapy in children undergoing hematopoietic stem cell transplantations-a feasibility study and randomized controlled trial. Support Care Cancer. 2020 Oct;28(10):4869-4879. doi: 10.1007/s00520-019-05258-2. Epub 2020 Jan 28.
Results Reference
derived

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Cryotherapy for Prevention of Oral Mucositis in Children Undergoing Hematopoietic Stem Cell Transplantation

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