No formal statistical hypothesis is planned.
ID
Bron
Verkorte titel
Aandoening
no disorders
Ondersteuning
Onderzoeksproduct en/of interventie
Uitkomstmaten
Primaire uitkomstmaten
Meaningfulness: The operator will rate the meaningfulness on a 11 point Scale.
Achtergrond van het onderzoek
Augmented Reality (AR) has the potential to improve the clinical workflow in the future by providing greater flexibility in the way users interact with the Philips Azurion system. AR allows flexible augmented display of 2D and 3D data overlaid or mixed with the real world. It offers more natural interaction, for instance by voice control or gesture interaction. The goal of this study is to investigate the user benefits and requirements for combining AR with Philips Azurion system and to study the possibilities how an AR head-mounted display (HMD) could be used together with the Philips Azurion system in Image Guided Therapies. The study is about an application research and not about patient research.
Doel van het onderzoek
No formal statistical hypothesis is planned.
Onderzoeksopzet
No follow-up is required per protocol. Patient will be followed according to regular clinical standard of care.
Onderzoeksproduct en/of interventie
N/A The study is not about patient research but application research.
Publiek
Peggy Goossen-Nachtigall
+31 6 110 343 34
peggy.nachtigall@philips.com
Wetenschappelijk
Peggy Goossen-Nachtigall
+31 6 110 343 34
peggy.nachtigall@philips.com
Belangrijkste voorwaarden om deel te mogen nemen (Inclusiecriteria)
- Operators who are certified IR/IOs, performing interventional vascular and oncology procedure
- Operators that are 18 years of age or older, or of legal age to give informed consent per state or national law.
- Procedures taken place in the angiography suite, with the same criteria as for the normal procedures that are not limited to standard angiographic I/O procedures and Image-Guided drainages using ultrasound or fluoroscopy.
- Patients elected for the procedures described, that are able to give informed consent per state or national law.
Belangrijkste redenen om niet deel te kunnen nemen (Exclusiecriteria)
- Operator or subject is Philips employee or their family members residing with this Philips employee.
- Operators that wear normal eye wear that do not fit underneath the AR HMD.
- Operators that are color blind and or have strabismus as eye deficiencies.
- All vulnerable subjects such as subjects lacking the capacity to provide consent, patients in emergency situations, pregnant or breast feeding women, or any other subject who meets an exclusion criteria, according to applicable national laws, if any.
Opzet
Deelname
Voornemen beschikbaar stellen Individuele Patiënten Data (IPD)
Toelichting
Opgevolgd door onderstaande (mogelijk meer actuele) registratie
Geen registraties gevonden.
Andere (mogelijk minder actuele) registraties in dit register
Geen registraties gevonden.
In overige registers
| Register | ID |
|---|---|
| NTR-new | NL9127 |
| Ander register | MEC-U : W20.089 |