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CSMed Wound Dressing on Radiation Dermatitis Clinical Trial
Investigate the effects of CSMed® for preventing and managing radiation dermatitis in patients with Breast cancer and Head-Neck cancer receiving radiotherapy (≥50 Gy).
A prospective study was conducted at the University Hospital Medical Center. The patient received part of the breast/neck skin CSMed® dressing or clinical routine skin care. Record the difference between the part of the skin with dressing and undressed skin for each patient. The severity of acute radiation dermatitis was graded using the RTOG clinical scoring standard. From the beginning of the treatment to 4 weeks after the end of the treatment, skin pain, itching, local fever and tightness, as well as skin healing time were collected every week.
Age
20 - 75 years
Sex
ALL
Healthy Volunteers
No
Chung Shan Medical University
Taichung, Taiwan
Start Date
June 1, 2020
Primary Completion Date
May 31, 2021
Completion Date
May 31, 2021
Last Updated
August 25, 2023
30
ACTUAL participants
CSMed Dressing
DRUG
Lead Sponsor
Chung Shan Medical University
NCT07081074
NCT03394417
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
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View ClinicalTrials.gov Terms and ConditionsNCT04173247