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A comparative study of the effect of Linora spray compared to the control group in patients with breast cancer treated with conformal radiotherapy

A comparative study of the effect of Linora spray compared to the control group in patients with breast cancer treated with conformal radiotherapy

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20201203049585N4
Enrollment
60
Registered
2024-03-30
Start date
2024-02-20
Completion date
Unknown
Last updated
2024-05-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Breast Cancer. Malignant neoplasm of breast

Interventions

Intervention 1: Intervention group: For the intervention group, at the time of starting radiotherapy, hydrocortisone ointment and Linora spray are applied to the place of radiotherapy for 2 times a da

Sponsors

Esfahan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: Breast cancer patients who underwent partial mastectomy Radiotherapy candidates are breast and lymph nodes

Exclusion criteria

Exclusion criteria: In case of allergy to the spray

Design outcomes

Primary

MeasureTime frame
Reduction of radiotherapy burn complications in breast cancer patients. Timepoint: The patients under study are examined in order to check the skin reactions in the first, third and end of the radiotherapy treatment. Method of measurement: The rate of skin reactions in people participating in this study is evaluated using the classification of world class skin complications of radiotherapy complications.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactNadia Najafizadeh

Esfahan University of Medical Sciences

Nadianajafizade@med.mui.ac.ir+98 31 3775 2366

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026