C10
Conditions
Interventions
Group 1: In patients receiving radiotherapy in the head and neck region, salivary flow rate, salivary pH, and questionnaires (oral health, salivary flow rate) are measured at T0, T1, T2, and T3.
Sponsors
UKB Poliklinik für Zahnärztliche Prothetik
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: Patients with oropharyngeal tumors (ICD C00–C10, C14) undergoing IMRT.
Exclusion criteria
Exclusion criteria: Lack of patient consent; Patients with dementia or other cognitive impairments who are unable to provide informed consent; Patients who decline participation in the study for other reasons
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Salivary flow rate, salivary pH, and questionnaires (VAS, Xerostomia Inventory, EORTC QLQ-C30) are assessed before IMRT (T0), after IMRT (T1), 3 months post-IMRT (T2), and 12 months post-IMRT (T3). | — |
Secondary
| Measure | Time frame |
|---|---|
| Submandibular, Sublingual, and Parotid Glands: Preserved or Resected, Radiation dose (Gy), Surgical report: Resection, Patient record: Medication list, Demographic data | — |
Countries
Germany
Contacts
Public ContactSabine Linsen
UKB Poliklinik für Zahnärztliche Prothetik
Outcome results
None listed