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Effect of Oral Cryotherapy and Normal Saline Mouth Rinse on Chemotherapy –Induced Oral Mucositis in Patients with Blood Stem-Cell Transplantatio

Not Applicable
Conditions
oral mucositis.
oral mucositis-ulcerative
Registration Number
IRCT201307165665N4
Lead Sponsor
ursing and Midwifery Faculty- Vice chancellor for research
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
60
Inclusion Criteria

Consciousness; Age between 18 to 70 years; To have Hodgkin's, non Hodgkin's lymphoma or Multiple Myeloma with the same grades; To have healthy oral mucous; Isolation of participants from the beginning of the project; To have Similar Chemotherapy properties; To have the same Autologous transplantation protocols
Exclusion criteria: Participants’ dissatisfaction; Loss of consciousness; Suffering from other diseases during treatment; use of narcotic analgesics continuously before the study; Combined therapies such as radiation therapy at the time of study; Fever, neutropenia and mucositis before starting treatment; To have respiratory diseases such as asthma and oral infections; Systemic diseases effective on oral tissues, especially periodontal disease; To have chemotherapy two weeks before transplantation; Change in treatment protocol during the study

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Oral Mucositis. Timepoint: before chemotherapy and 3rd, 7th, 14th and21th days folowing end of chemotherapy. Method of measurement: WHO Mucositis Scale.
Secondary Outcome Measures
NameTimeMethod
ausea and Vomiting. Timepoint: During 4 days, every day following end of chemotherapy. Method of measurement: checklist.
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