Savory effect of mucositis and pain severity in children receiving chemotherapy: a randomized double-blind clinical trial.
Phase 2
- Conditions
- Condition 1: mucosit. Condition 2: pain.Oral mucositis (ulcerative)Ocular pain
- Registration Number
- IRCT2016061813691N7
- Lead Sponsor
- Vice chancellor for research, Tabriz University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 60
Inclusion Criteria
Entry criteria: full consciousness, admitted to Tabriz Children's Hospital Hematology and Oncology, treatment with chemotherapy drugs cause mucositis (cisplatin, cyclophosphamide and Mtvtrvksayd); at least three years and a maximum of fourteen years, not having the recurrent infectious waste oral, diagnosis (ALL, lymphoma and neuroblastoma). Exclusion criteria: children and parents not wanting to continue working; the death of the child; the child is connected to the ventilator, continuous use painkillers or opiates to relieve pain.As a result the treatment will be compared in the two groups that could be a less costly and less complications used to treat and prevent oral ulcers.
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Mucositis. Timepoint: For five days following chemotherapy with oral ulcers. Method of measurement: Czech List View and questionnaire oral ulcers World Health Organization.
- Secondary Outcome Measures
Name Time Method Pain. Timepoint: For five days following chemotherapy with oral ulcers. Method of measurement: Czech List View and tools Ocher pain.