Breast cancer. Malignant neoplasm of unspecified site of unspecified female breast
Conditions
Interventions
Intervention 1: Control group: In breast cancer patients will first have a blood sample taken as a control. Then, for one month, a topical medication containing sweet almond will be applied twice dai
Sponsors
Sabzevar University of Medical Sciences
Eligibility
Sex/Gender
Female
Age
18 Years to 65 Years
Inclusion criteria
Inclusion criteria: Consent to participate in the study Absence of metastasis at diagnosis Anatomopathological diagnosis of breast cancer Age range 18 to 65 years Absence of violet oil, topical almond oil at the time of entry into the study
Exclusion criteria
Exclusion criteria: Non-breast cancers Use of violet oil, topical almond oil at the time of entry into the study
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| IL- 1ß. Timepoint: Before and after the intervention. Method of measurement: Measuring the amount in the patient's blood.;IL- 4. Timepoint: Before and after the intervention. Method of measurement: Measuring the amount in the patient's blood.;TNF-a. Timepoint: Before and after the intervention. Method of measurement: Measuring the amount in the patient's blood. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactSeyed Majid Ghazanfari
Sabzevar University of Medical Sciences
Outcome results
None listed