Actively Recruiting
Gender-specific Preoperative Anxiety Level and Postoperative Opioid Requirement After ENT Surgery.
Led by Medical University of Vienna · Updated on 2025-07-04
300
Participants Needed
1
Research Sites
267 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
The study will be designed to investigate the impact of the preoperative anxiety level on postoperative opioid requirement during the PACU stay, in order to improve postoperative pain treatment in the long term after ENT surgery. The present study can contribute to improve postoperative pain management in patients in the field of ENT surgery, as new influencing parameters and risk factors may be discovered.
CONDITIONS
Official Title
Gender-specific Preoperative Anxiety Level and Postoperative Opioid Requirement After ENT Surgery.
Who Can Participate
Eligibility Criteria
You may qualify if you...
- American Society of Anesthesiology (ASA) physical status I-IV
- Able to read and understand the information sheet and to sign the consent form
- Scheduled for elective ENT surgery under general anesthesia
- Written informed consent
- Age 18 years or older
You will not qualify if you...
- Difficulty understanding study procedures, pain scoring systems, or questionnaires
- Surgical procedure requiring elective postoperative ventilation
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Medical University Vienna
Vienna, State of Vienna, Austria, 1090
Actively Recruiting
Research Team
M
Marita Windpassinger, MD
CONTACT
O
Olga Plattner, MD
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
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