R13 G20 G21
Conditions
Interventions
Group 1: Observational study: Questionnaire taken after taking the 3D-printed tablet compared to a standard tablet
Repeated intake/one-time questionnaire survey
Sponsors
Helios Klinikum Erfurt GmbH
Eligibility
Sex/Gender
All
Age
50 Years to No maximum
Inclusion criteria
Inclusion criteria: patients with prescription for amlodipine 5 mg or ramipril 5 mg or spironolactone 12,5 mg or spironolactone 25 mg; hospitalized patients
Exclusion criteria
Exclusion criteria: Age < 50 years
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Reaching the planned number of 450-480 patients Investigation of the acceptance of a new galenic dosage form (3D-printed tablet) in a geriatric/neurological patient cohort | — |
Countries
Germany
Contacts
Public ContactJana Giesel-Gerstmeier
Helios Kliniken GmbH
Outcome results
None listed