Patients with solid tumours
Conditions
Interventions
Group 1: Patients with solid tumours. The occurrence of potential interactions between dietary supplements and oncological pharmacotherapies is being investigated.
Sponsors
Institut für Ernährungsmedizin, Universität zu Lübeck
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: Diagnosis of a solid tumour outpatient or inpatient oncologic pharmacotherapy
Exclusion criteria
Exclusion criteria: Dementia comorbidities Expected life expectancy of < 6 months
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Prevalence of interactions between dietary supplements and oncological pharmacotherapy (in percent) at the time of oncological therapy | — |
Secondary
| Measure | Time frame |
|---|---|
| - Prevalence of interactions between dietary supplements (DS) and oncological pharmacotherapy in DS users - Frequency of need for medical intervention due to detected interactions - Prevalence of interactions between DS and the complete (also non-oncological) medication - Influence of other variables on the occurrence of interactions between DS and oncological pharmacotherapy as well as the complete medication (Age, sex, tumour entity, comorbidities, total number of drugs taken, type and total number of DS taken) - Patients‘ quality of life (using EORTC QLQ-C30 Version 3.0) - Motivation for taking DS | — |
Countries
Germany
Contacts
Public ContactMartin Smollich
Institut für Ernährungsmedizin, Universität zu Lübeck
Outcome results
None listed