Condition: Head and Neck Cancers · Acute Radiation Dermatitis · Sponsor: National University Hospital, Singapore
This is a phase IV, prospective, double-blind, randomized controlled trial with 2 study arms. The study population will be patients receiving chemoradiation for head and neck carcinomas, the majority of whom will be outpatients unless they require inpatient supportive care during treatment. There will be a 12 to 14-week longitudinal follow-up with 9 assessments conducted during this follow-up. The estimated duration of recruitment will be 6-8 years. Intervention group If a patient is allocated to the intervention group following randomization, the patient will be treated with StrataXRT. Control group If a patient is allocated to the control group following randomization, the patient will be treated with standard clinical practice which consists of aqueous cream.
This description comes directly from the study's public registry record.
David Chia · 67737888 · david_chia@nuhs.edu.sg
Fatin Aliyah Binte Hussin · 67723079 · fatin_hussin@nuhs.edu.sg
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| National University Hospital | Singapore, Singapore | Recruiting |
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Source record: clinicaltrials.gov/study/NCT03394417