Gender-specific Preoperative Anxiety Level and Postoperative Opioid Requirement After ENT Surgery.
Recruiting · NCT05141591 · Observational (researchers observe without assigning treatment) · Lead sponsor: Medical University of Vienna
View the official record on ClinicalTrials.gov →Interventions studied
Anxiety level assessment
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.
Who can take part
Age range
18 Years and older
Sex
All (male and female)
Healthy volunteers
Yes - healthy volunteers may be accepted
Phase
Not specified
Study type
Observational (researchers observe without assigning treatment)
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 is running
1 location listed.
- Medical University Vienna - Vienna, State of Vienna, Austria