Skip to content

Azurion AR (Augmented Reality) study

Azurion AR (Augmented Reality) study

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON22889
Enrollment
4
Registered
2020-12-15
Start date
2020-12-15
Completion date
Unknown
Last updated
2024-02-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

no disorders

Interventions

N/A The study is not about patient research but application research.

Sponsors

Philips Medical Systems Nederland B.V.
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: - 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.

Exclusion criteria

Exclusion criteria: - 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.

Design outcomes

Primary

MeasureTime frame
Meaningfulness: The operator will rate the meaningfulness on a 11 point Scale.

Secondary

MeasureTime frame
- Usability: The operator will rate the usability of the Azurion AR. It will be assessed by using the System Usability Score (SUS). - Image quality: The operator will rate the image quality of the virtually presented medical images on a 5 point Likert Scale. - Ergonomics: The operator will indicate to what extend he/she is affected by 17 prompted symptoms using the visual fatigue questionnaire. - Workload: The operator will fill out a task load questionnaire, the raw version of the NASA Task Load Index (TLX) to assess the workload on six subscales with 21 gradations.

Contacts

Public ContactPeggy Goossen-Nachtigall

Philips Medical Systems Nederland B.V.

peggy.nachtigall@philips.com+31 6 110 343 34

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)