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Implementation of a bundle of non-pharmacological interventions aimed at stress reduction in the PACU: effects on pain and use of opioids

Conditions
Surgical population
Registration Number
NL-OMON23536
Lead Sponsor
Investigator initiated
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Pending
Sex
Not specified
Target Recruitment
1066
Inclusion Criteria

Patients from all surgical disciplines undergoing surgery with a minimum duration of 2 hours and a minimal hospital length of stay of 1 postoperative night will be eligible for inclusion.

Exclusion Criteria

Use of neuraxial anesthesia or analgesia, a history of psychiatric illness, chronic pain conditions or chronic use of opioids.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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