Patients undergoing chemotherapy with oral mucositis. Oral mucositis (ulcerative)
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: All patients undergoing chemotherapy and having oral mucositis Complete satisfaction to participate in research and completion and to sign a form of informed consent The health of oral mucosa before chemotherapy Absence of autoimmune diseases Untreated combined therapy, such as radiation therapy Do not use mouthwash and antibiotic drugs before doing research Earn less than 70 points based on the quality of life associated with oral health
Exclusion criteria
Exclusion criteria: Unwillingness to participate in research Do radiotherapy
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Oral Mucositis. Timepoint: The beginning of the study (before the intervention) and 7, 14 and 21 days after starting the mouthwash. Method of measurement: The WHO benchmark for oral mucositis is used. | — |
Secondary
| Measure | Time frame |
|---|---|
| Oral Health-related quality of life. Timepoint: At the beginning of the study (baseline) and 7, 14 and 21 days after the start of mouthwash. Method of measurement: The quality of life related oral health questionnaire will be used to assess Oral Health-related quality of life. | — |
Countries
Iran (Islamic Republic of)
Contacts
Yasouj University of Medical Sciences