I67.10 I67.11
Conditions
Interventions
Group 1: Questionnaire for patients before and after demonstration of 3D model for pre-treatment consultation
Sponsors
Universitätsklinikum Leipzig
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: - Neurovascular pathologies to be treated electively - Written consent to study available - Study participants >/= 18 years - Indication for interventional or surgical treatment of the intracranial vascular change given by the treating physicians in neuroradiology or neurosurgery.
Exclusion criteria
Exclusion criteria: - Neurovascular pathologies requiring emergency care - Written consent to study is missing - Study participants < 18 years - Contraindications for interventional or surgical treatment of the intracranial vascular change by the treating physicians in neuroradiology or neurosurgery.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The primary endpoint is the investigation of improved information transfer between doctor and patient through the patient-specific 3D models, especially with regard to understanding their own disease, the impact on lifestyle and the planned therapy. | — |
Secondary
| Measure | Time frame |
|---|---|
| The costs and the time required for building and printing of the 3D models are to be recorded as secondary endpoints and a statement is to be made about the applicability in relation to the benefit in everyday clinical practice. | — |
Countries
Germany
Contacts
Public ContactFranziska Frank
Universitätsklinikum Leipzig
Outcome results
None listed