Cancer patients undergoing chemotherapy.
Conditions
Interventions
Intervention 1: Intervention group: The mouthwash containing Syzygium aromaticum (5%) and Commiphora molmol (5%) 5 ml three times a day. Intervention 2: Control group: The protact mouthwash 5 ml three
Sponsors
Sari University of Medical Sciences
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: Age =18 years of age Willing to provide written informed consent First and second grade of chemotherapy-induced mucositis
Exclusion criteria
Exclusion criteria:
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Primary outcome measures included improvement or termination of mucositis. Timepoint: At the beginning of treatment (day 1) and then on days 3, 5, 7 and 10. Method of measurement: Mucositis severity based on Common Terminology Criteria for Adverse Events and World Health Organization Criteria. | — |
Secondary
| Measure | Time frame |
|---|---|
| Pain severity. Timepoint: Days 1, 3, 5, 7, 10. Method of measurement: Based on the pain severity according to Visual Analogue Scale. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactEbrahim salehifar
Sari University of Medical Sciences
Outcome results
None listed