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Clinical Trials/NL-OMON23536
NL-OMON23536
Not yet recruiting
Not Applicable

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

Investigator initiated0 sites1,066 target enrollmentTBD

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Surgical population
Sponsor
Investigator initiated
Enrollment
1066
Status
Not yet recruiting
Last Updated
2 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
2 years ago
Study Type
Interventional

Investigators

Sponsor
Investigator initiated

Eligibility Criteria

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.

Outcomes

Primary Outcomes

Not specified

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