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Neoviderm Skin Emulsion in the Prevention of Radiation Dermatitis

Phase 2
Terminated
Conditions
Head and Neck Cancer
Breast Cancer
Registration Number
NCT01701466
Lead Sponsor
Sir Mortimer B. Davis - Jewish General Hospital
Brief Summary

The purpose of this study is to determine whether NeoVIDERM is effective at preventing radiation dermatitis in patients receiving external beam radiation therapy to the head and neck or breast areas.

Detailed Description

Not available

Recruitment & Eligibility

Status
TERMINATED
Sex
All
Target Recruitment
14
Inclusion Criteria

Not provided

Exclusion Criteria

Not provided

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Primary Outcome Measures
NameTimeMethod
Maximum skin toxicity7 weeks post beginning of radiation treatments

The objective of this study is to determine the occurrence and degree of acute skin toxicity in patients receiving radical radiation therapy with preventive application of neoVIDERM compared to patients treated with institutional standard skin care.

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Jewish General Hospital

🇨🇦

Montreal, Quebec, Canada

Jewish General Hospital
🇨🇦Montreal, Quebec, Canada

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