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Clinical Trials/ISRCTN84820314
ISRCTN84820314
Unknown
未知

Effectiveness of an audio-visual device for anxiety and pain reduction during a nerve block procedure – a randomized controlled trial

Spaarne Gasthuis0 sites99 target enrollmentJuly 6, 2021

Overview

Phase
未知
Intervention
Not specified
Conditions
Pain and anxiety before and during a nerve block procedure
Sponsor
Spaarne Gasthuis
Enrollment
99
Last Updated
4 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
July 6, 2021
End Date
February 2, 2019
Last Updated
4 years ago
Study Type
Interventional
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • 1\. Adults 18 years and older
  • 2\. Conditions that require nerve block intervention
  • 3\. Written informed consent
  • 4\. We allow re\-enrolment in the randomisation procedure, as some patients will return for repeated treatment during the randomisation period. A new written informed consent is needed

Exclusion Criteria

  • 1\. Patients with difficulties in speaking and reading Dutch
  • 2\. Patients physically or mentally not able to consent
  • 3\. Patients with severe hearing loss or refraction errors making it impossible to wear the audiovisual device
  • 4\. Anxiety disorders, such as panic disorder, obsessive\-compulsive disorder, posttraumatic stress disorder and others
  • 5\. ASA 4 \- 5

Outcomes

Primary Outcomes

Not specified

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