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Investigation of Pain and Anxiety in INterventional Radiology

Investigation of Pain and Anxiety in INterventional Radiology - iPAIN

Status
Unknown
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON45296
Enrollment
2000
Registered
2017-04-11
Start date
Unknown
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

Periprocedural pain

Interventions

Anxiety
Intervention
Pain
Radiology

Sponsors

Universitair Medisch Centrum Utrecht
Lead Sponsor

Eligibility

Age
18 Years to 64 Years

Inclusion criteria

Inclusion criteria: In order to be eligible to participate in this study, a subject must undergo a radiological procedure. As pain or anxiety is highly variable, there is no a priori limitation to particular procedures.

Exclusion criteria

Exclusion criteria: - Less than 18 years of age; - Not being capable of giving informed consent.

Design outcomes

Primary

MeasureTime frame
The pain is measured using a numeric rating scale (NRS) and anxiety using the Richmond agiation-sedation scale (RASS) during the intervention, as part of standard clinical practice.—

Secondary

MeasureTime frame
Not applicable.—

Countries

The Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)