search
Back to results

Topical Use of Difinsa53™ to Prevent Radiation Dermatitis

Primary Purpose

Radiodermatitis

Status
Terminated
Phase
Phase 1
Locations
United States
Study Type
Interventional
Intervention
Difinsa53
Aquaphor
Sponsored by
ProTechSure Scientific, Inc.
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Radiodermatitis focused on measuring breast cancer, radiation, dermatitis

Eligibility Criteria

undefined - undefined (Child, Adult, Older Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria:

  • Female patients 18 years and older
  • Pathologic diagnosis of breast cancer requiring radiation therapy to whole breast
  • Able to apply lotion to treatment area at least twice daily during radiation course
  • All surgical sites healed
  • No evidence of infection
  • No history of sensitivity to any component in Aquaphor or Difensa53

Exclusion Criteria:

  • Prior history of radiation therapy (RT) to that site
  • Known dermatologic conditions affecting skin in radiation port
  • Concurrent chemotherapy
  • Skin infection in radiation port
  • History of sensitivity to Aquaphor or Difensa53 component

Sites / Locations

  • Poudre Valley Health System

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Single Arm

Arm Description

Radiation field is divided into two sections, one treated with Difinsa53 and the other with Aquaphor

Outcomes

Primary Outcome Measures

Radiation Dermatitis as Determined by Radiation Therapy Oncology Group (RTOG) Acute Radiation Morbidity Scoring Criteria
A blinded observer will quantify degree of dermatitis assigning each half of the radiation field a score from 0 to 4. 0 represents no dermatitis and 4 is severe dermatitis using the RTOG scoring criteria.

Secondary Outcome Measures

Full Information

First Posted
August 19, 2015
Last Updated
October 4, 2017
Sponsor
ProTechSure Scientific, Inc.
Collaborators
Poudre Valley Health System
search

1. Study Identification

Unique Protocol Identification Number
NCT02534129
Brief Title
Topical Use of Difinsa53™ to Prevent Radiation Dermatitis
Official Title
Topical Use of a Silibin-based Cream, Difinsa53™, to Prevent Radiation Dermatitis in Patients With Breast Cancer: A Prospective Study
Study Type
Interventional

2. Study Status

Record Verification Date
October 2017
Overall Recruitment Status
Terminated
Why Stopped
Insufficient dermatitis was seen in the controls to allow any determination of protection by Difinsa53
Study Start Date
August 2015 (undefined)
Primary Completion Date
March 2016 (Actual)
Study Completion Date
March 2016 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
ProTechSure Scientific, Inc.
Collaborators
Poudre Valley Health System

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Phase II trial of the silibin containing cream, Difinsa53 to determine efficacy in delaying, ameliorating, or preventing radiation dermatitis in patients with breast cancer undergoing whole breast radiation.
Detailed Description
The proposed study seeks to evaluate the efficacy of DIFINISA53™, a safe silibin-based skin cream, on preventing radiation dermatitis (RD) when compared to an over the counter ointment, Aquaphor, in women undergoing radiation therapy for breast cancer following lumpectomy or mastectomy surgery. Presently there is no known fully effective topical protectant from RD and there is no consensus among radiation oncologists on how best to treat RD. This study seeks to identify a more effective option for patients receiving radiation therapy. Each participant will apply the DIFINISA53™ cream to one area of the treated skin and Aquaphor to another area of treated skin. Skin reactions will be evaluated using medical professional assessment, participant assessment, and photographic assessment by a third party.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Radiodermatitis
Keywords
breast cancer, radiation, dermatitis

7. Study Design

Primary Purpose
Prevention
Study Phase
Phase 1, Phase 2
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
13 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Single Arm
Arm Type
Experimental
Arm Description
Radiation field is divided into two sections, one treated with Difinsa53 and the other with Aquaphor
Intervention Type
Drug
Intervention Name(s)
Difinsa53
Other Intervention Name(s)
Dimethicone
Intervention Description
Difinsa53 cream is applied to one half of radiation field
Intervention Type
Drug
Intervention Name(s)
Aquaphor
Other Intervention Name(s)
petrolatum
Intervention Description
Aquaphor is applied to one half of radiation field
Primary Outcome Measure Information:
Title
Radiation Dermatitis as Determined by Radiation Therapy Oncology Group (RTOG) Acute Radiation Morbidity Scoring Criteria
Description
A blinded observer will quantify degree of dermatitis assigning each half of the radiation field a score from 0 to 4. 0 represents no dermatitis and 4 is severe dermatitis using the RTOG scoring criteria.
Time Frame
8 weeks

10. Eligibility

Sex
Female
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Female patients 18 years and older Pathologic diagnosis of breast cancer requiring radiation therapy to whole breast Able to apply lotion to treatment area at least twice daily during radiation course All surgical sites healed No evidence of infection No history of sensitivity to any component in Aquaphor or Difensa53 Exclusion Criteria: Prior history of radiation therapy (RT) to that site Known dermatologic conditions affecting skin in radiation port Concurrent chemotherapy Skin infection in radiation port History of sensitivity to Aquaphor or Difensa53 component
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Joshua Petit, MD
Organizational Affiliation
UC Health, Poudre Valley Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Poudre Valley Health System
City
Fort Collins
State/Province
Colorado
ZIP/Postal Code
80528
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
21514477
Citation
McQuestion M. Evidence-based skin care management in radiation therapy: clinical update. Semin Oncol Nurs. 2011 May;27(2):e1-17. doi: 10.1016/j.soncn.2011.02.009.
Results Reference
background
PubMed Identifier
21786113
Citation
Becker-Schiebe M, Mengs U, Schaefer M, Bulitta M, Hoffmann W. Topical use of a silymarin-based preparation to prevent radiodermatitis : results of a prospective study in breast cancer patients. Strahlenther Onkol. 2011 Aug;187(8):485-91. doi: 10.1007/s00066-011-2204-z. Epub 2011 Jul 22.
Results Reference
background

Learn more about this trial

Topical Use of Difinsa53™ to Prevent Radiation Dermatitis

We'll reach out to this number within 24 hrs