Topical Doxepin for Radiation-induced Dermatitis

Breast Cancer Clinical Trial

Official title:

Topical Doxepin for Prevention and Management of Radiation-induced Dermatitis

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT02447211
• Other study ID #: 900
• Status: Recruiting
• Phase: Phase 2
• Start date: May 2015
• Est. completion date: January 2019

Study information

• Verified date: January 2019
• Source: Isfahan University of Medical Sciences
• Contact: Golnaz Vaseghi, Ph.D
• Phone: 0989133259802
• Email: golnazvaseghi[@]yahoo.com
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Radiation dermatitis is one of the most common side effects of radiotherapy approximately occurring in about 95% of patients receiving radiotherapy . Acute injury due to structural tissue damage, generation of free radicals, irreversible double-stranded breaks in nuclear and mitochondrial DNA, and initiation of an inflammatory response in the epidermis and dermis occurs within hours to weeks after radiation exposure. Radiation dermatitis due to pain and discomfort has an adverse impact on the quality of a patient's life.The radiation toxicities such as radiation dermatitis encountered in clinical practice are typically managed with a variety of topical agents such as water-based moisturizing creams or lotions, topical steroids, antiinflammatory emulsions, and wound dressings. Pharmacologic interventions for the prevention and treatment of these toxicity can be used to protect skin against radiation damage.Currently, there is no standard treatment for the prevention of radiation-induced dermatitis with demonstrated effectiveness.The aim of this randomized, double-blind, placebo-controlled study is to evaluate the effectiveness of topical doxepin for the prevention and management of radiation-induced dermatitis during postoperative radiotherapy for breast cancer.

Description:

The patients who have undergone breast surgery and require radiotherapy and fulfill the inclusion criteria of the study will be entered the study. All the patients will be treated by 3D conformal radiation therapy using CT -based treatment planning and multi leaf linear accelerators. The patients will be treated by conventional fractionation regimens to a total dose of 5000 cGy (25 fractions of 200 cGy, 5 days per week). Every week the patients will be visited by an experienced radiation oncologist and the skin reaction will be determined and recorded according to RTOG Acute Radiation Morbidity Scoring Criteria which scores from 0 to 4. The patients receive Doxepin cream at the beginning of 5th week of radiotherapy and use it for a whole week. After acquiring written permission, the radiotherapy site will be photographed at the start and ending of the Doxepin

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 60
• Est. completion date: January 2019
• Est. primary completion date: January 2019
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: Female
• Age group: 21 Years to 65 Years

Eligibility

Inclusion Criteria:

• Female with a diagnosis of, breast adenocarcinoma and be referred for post-operative radiotherapy with or without concurrent chemotherapy and with or without mastectomy

• Participants must not be pregnant.

• Participants treated with a total dose of 5000 cGy (25 fractions of 200 cGy, 5 days per week

Exclusion Criteria:

• Patients who are not eligible

• The presence of skin diseases in the radiation area

• Patients have constipation, xerostomia, blurred vision, urinary retention

• Hypersensitivity to doxepin

Related Conditions & MeSH terms

• Breast Cancer
• Dermatitis
• Radiodermatitis

Intervention

Drug:
• Doxepin cream 5%
Patients use doxepin creamtwice daily for one weeks

Other:
• Placebo
Patients use cream without doxepin ingredient twice daily for one weeks

Locations

Country	Name	City	State
Iran, Islamic Republic of	Isfahan University of Medical Sciences	Isfahan

Sponsors (1)

Lead Sponsor	Collaborator
Isfahan University of Medical Sciences

Country where clinical trial is conducted

Iran, Islamic Republic of, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Grading of dermatitis was performed according to the Radiation Therapy Oncology Group acute radiation morbidity scoring criteria	at the beginning of 5th week of radiotherapy and use it for two weeks	At the beginning of 5th week of radiotherapy to two weeks