Overview
Dermaprazole Cream for Radiation Dermatitis in Definitive Head and Neck Cancer
Status:
Not yet recruiting
Not yet recruiting
Trial end date:
2027-09-01
2027-09-01
Target enrollment:
0
0
Participant gender:
All
All
Summary
In this study, the study team seek to conduct a pilot clinical study to evaluate the safety and efficacy of a reformulated proton pump inhibitor (PPI) cream (Dermaprazole) in definitive head and neck cancer (HNC) patients.Phase:
Phase 2Accepts Healthy Volunteers?
NoDetails
Lead Sponsor:
Mohamad Hassan FakhreddineTreatments:
Esomeprazole
Criteria
Inclusion Criteria:- Patients with head and neck malignancy (including radiation therapy to primary head
cancers of any histology and/or neck lymphatics, excluding brain malignancies)
- Biopsy proven diagnosis of head and neck malignancy
- Planned to receive definitive chemoradiation of at least 66Gy
- Age 18 years or older
- Eastern Cooperative Oncology Group (ECOG) performance status 0 - 2
- Written Informed Consent
- History and Physical within 12 weeks of enrollment
Exclusion Criteria:
- Prior head and neck radiotherapy
- Neoadjuvant chemotherapy
- Any serious medical condition or illness that would preclude the safe administration
of the trial treatment including, but not limited to, active infection, symptomatic
heart failure, unstable angina, psychiatric illness or social situations that would
limit compliance with treatment
- Currently taking proton pump inhibitors. Eligible if discontinues with physician
approval.
- Lack of concurrent chemotherapy
- Open wound at time of simulation
- Known autoimmune, connective tissue, or skin disorder; or other theoretical
radiosensitivity to include bullous pemphigoid, dermatomyositis, lupus of the skin and
scleroderma