Investigation of Pain and Anxiety in INterventional Radiology

Withdrawn

• Conditions: Periprocedural pain; 10043413

• Registration Number: NL-OMON45296
• Lead Sponsor: niversitair Medisch Centrum Utrecht

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 28 February 2024

Recruitment & Eligibility

• Status: Withdrawn
• Sex: Not specified
• Target Recruitment: 2000

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

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

Study & Design

• Study Type: Observational non invasive
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
<p>The pain is measured using a numeric rating scale (NRS) and anxiety using the<br /><br>Richmond agiation-sedation scale (RASS) during the intervention, as part of<br /><br>standard clinical practice. </p><br>

Secondary Outcome Measures

Name	Time	Method
<p>Not applicable.</p><br>