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Comparison study between chamomile and calendula creams to prevent radiation-induced skin lesions

Not Applicable
Recruiting
Conditions
wounds and injuries
Registration Number
RBR-98myd6
Lead Sponsor
Daniele Machado Oliveira Andrade
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
Not specified
Target Recruitment
Not specified
Inclusion Criteria

Both sexes; age equal to or over 18 years; diagnosis of head and neck cancer

Exclusion Criteria

History of radiotherapy in the same field of treatment; previous report of allergic reaction to chamomile or calendula

Study & Design

Study Type
Intervention
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
To compose the sample, all patients treated at the two radiotherapy services were considered for a period of 6 (six) months. It is estimated that in this period, based on the history of the services, about 50 patients will be evaluated.
Secondary Outcome Measures
NameTimeMethod
Both groups using chamomile cream and calendula cream are expected to have low incidences in the development of radiodermatitis and skin toxicity grades.
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