Patient-specific 3D models to improve doctor-patient communicatio

Conditions: I67.10
I67.11

Registration Number: DRKS00027893

Lead Sponsor: niversitätsklinikum Leipzig

Brief Summary: Not available

Detailed Description: Not available

Recruitment & Eligibility

Status: Pending

Sex: All

Target Recruitment: 24

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

- 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.

Study & Design

Study Type: observational

Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
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 Outcome Measures

Name	Time	Method
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.