Affect of Achillea millefolium in Prophylaxis of oral mucositis
Not Applicable
- Conditions
- Oral mucositis.Oral mucositis (ulcerative)
- Registration Number
- IRCT201309215704N2
- Lead Sponsor
- Hematology and Oncology Research Center, Tabriz University of Medical Sciences, Iran
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 18
Inclusion Criteria
AML patients including both male or female ones, aged between 16-85 who are candidate for chemotherapy;
Exclusion criteria: Pregnancy; Patients who are not volunteer; Patients with less than 3 weeks duration of hospitalization; Patients with mucositis
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Duration of mucositis. Timepoint: From begining of chemotherapy until 21 days later. Method of measurement: Counting number of days.;Severity of mucositis. Timepoint: First day of chemotherapy until 21 days later. Method of measurement: WHO oral mucositis scale.
- Secondary Outcome Measures
Name Time Method Amount of analgesics requested for pain caused by mouth sores. Timepoint: First day of chemotherapy until 21 days later. Method of measurement: Type and dosage of analgesics recorded in patients records in 21 days duration.