Impact of preoperative anxiety on opioid use after ENT surgery

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This study investigates how preoperative anxiety levels affect the need for opioids during recovery after elective ENT surgery. It utilizes validated questionnaires to assess anxiety in patients scheduled for surgery, aiming to identify psychological factors that may influence postoperative pain management. By understanding these relationships, the study seeks to improve personalized pain treatment strategies for patients undergoing ENT procedures.

Why it matters

Who can join: the full rules

Inclusion Criteria:

* American Society of Anesthesiology (ASA) physical status I-IV
* able to read and understand the information sheet and to sign the consent form
* being scheduled for elective ENT surgery under general anesthesia
* written informed consent
* age≥18 years

Exclusion Criteria:

* difficulty to understand study procedure, pain scoring system or questionnaires
* surgical procedure warranting elective postoperative ventilation

Where it's running

• Medical University Vienna
  Vienna, State of Vienna, Austria Recruiting

Study contacts

• Study coordinator: Marita Windpassinger, MD
• Email: marita.windpassinger@meduniwien.ac.at
• Phone: +43 1 40400 41020

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.