radiation therapy-induced dermatitis. Radiodermatitis, unspecified
Conditions
Interventions
Intervention 1: Intervention group: Intervention group: The medicine of the intervention group is hydrogel, which includes marigold, marshmallow, and honey. This topical skin hydrogel will be made by
Sponsors
Sabzevar University of Medical Sciences
Eligibility
Sex/Gender
All
Age
45 Years to 75 Years
Inclusion criteria
Inclusion criteria: Consent to participate in the study Mental and intellectual health Radiotherapy candidate Staying in Bezvar and suburbs (all meetings should be held in Bezvar) Age range 45-70 years Absence of underlying chronic disease: dermatology, lupus, active scleroderma, underlying allergy, diabetes, and chronic kidney disease No smoking, drugs and alcohol
Exclusion criteria
Exclusion criteria: People who have changed their place of residence since the middle of the study Do not agree to continue participating in the project from the middle of the study suffer severe complications from radiotherapy. Changing the patient's treatment method from the middle of the treatment process Failure to use plan drugs have allergies to study drugs
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Dermatitis. Timepoint: Day 0 (day of starting radiation therapy and start of intervention) and days 7-14-21 after the treatment and one month after the end of the treatment to check acute dermatitis and 3 months after the end of treatment to check sub-acute dermatitis. Method of measurement: CTCAE v5.0. | — |
Secondary
| Measure | Time frame |
|---|---|
| Itching. Timepoint: (From start of intervention) to day 7-21-28 (from the start of radiotherapy once a week). Method of measurement: self expression.;Erythema. Timepoint: (From start of intervention) to day 7-21-28 (from the start of radiotherapy once a week). Method of measurement: view. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactAtefeh Asadi
Sabzevar University of Medical Sciences
Outcome results
None listed