Gallic Acid
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Patients over 20 years of age. Both sexes. Diagnosis and treatment of head and neck cancer in a hospital participating in the study. Participation voluntarily authorized through signing of the Free and Informed Consent Form. Presence on the scheduled days for data collection and nutritional assessment
Exclusion criteria
Exclusion criteria: Patients who discontinue cancer treatment or do not follow the instructions related to the use of the dietary supplement. Patients with allergies or intolerance to any ingredient of the formula. Diabetic patients. Patients using feeding tubes. Oncology patients with neoplasms in anatomical sites other than the head and neck. Patients not identified by the researchers. Patients who refuse to participate or have not signed the Free and Informed Consent Form
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To evaluate the role of gallic acid in the modulation of molecular, biochemical, and morphological parameters in patients with head and neck cancer through the analysis of inflammatory, antioxidant, and nutritional biomarkers collected before and after the nutritional intervention with the dietary supplement containing gallic acid | — |
Secondary
| Measure | Time frame |
|---|---|
| It is expected that the use of the dietary supplement with the addition of gallic acid will be able to modulate squamous cells in patients with head and neck cancer influencing morphological molecular and nutritional parameters evaluated before and after the nutritional intervention and contributing to increased survival rates and improved patient well-being | — |
Countries
Brazil
Contacts
Universidade Estadual de Montes Claros