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A study on the role of traditional drug based dressings in the treatment of skin wounds produced in breast cancer patients undergoing radiotherapy

Phase 3
Completed
Conditions
Health Condition 1: C508- Malignant neoplasm of overlappingsites of breast
Registration Number
CTRI/2020/11/029311
Lead Sponsor
I
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
Not specified
Target Recruitment
110
Inclusion Criteria

1.Patient willing to give written informed consent form

2. Newly diagnosed with non metastatic breast cancer and undergoing adjuvant radiation for breast cancer who develop grade III radiation therapy induced moist desquamation

Exclusion Criteria

1.Patient unwilling to take part in study

2.Patients with contraindications for Radiation therapy

3.Patients with radiation skin reactions of severity less than Grade III

4.Patients with pre existing skin conditions such as psoriasis, eczema, or connective tissue disorders or history of allergy to components used in trial dressings

5.Patients on steroids or immunosuppressant therapy

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
<br/ ><br>To assess tolerance of Acalypha indica impregnated thin film on radiated tissue <br/ ><br>Timepoint: 4th to 6th week of radiation treatment for each patient.
Secondary Outcome Measures
NameTimeMethod
To assess wound healing capacity of Acalypha indica impregnated thin film on radiation induced dermatitis wounds with respect to time taken for complete wound healing in comparison to gentian violet topical application. <br/ ><br>To assess improvement in quality of life of patientsTimepoint: Upto 6 months after completion of radiation protocol of last recruited patient
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