The DICTION study
Recruiting
- Conditions
- Postoperative pain
- Registration Number
- NL-OMON21888
- Lead Sponsor
- Department of Anesthesiology, Amsterdam UMC, location AMC
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Not specified
- Target Recruitment
- 250
Inclusion Criteria
Aged eighteen years or older
-Fluent in Dutch
-Capable of completing the OBAS questionnaire
-Has no objection to study inclusion
-Underwent elective surgery that required overnight hospitalization
-The performed surgery was orthopedic, trauma surgical, neurosurgical, abdominal or obstetric in nature
Exclusion Criteria
-ASA 5 or higher
-Emergency surgery
-Hospitalization at the intensive care unit (ICU), or previous admission to the ICU during the same hospital admission
Study & Design
- Study Type
- Observational non invasive
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The main study endpoint is the description of the psychometric properties of the optimized Dutch OBAS.
- Secondary Outcome Measures
Name Time Method Secondary endpoints are determination of the MCID and clinical usability