Postoperative pain relief following pancreaticoduodenectomy: Triple P (PostPainPan) Study
Phase 4
Completed
- Conditions
- postoperatieve pijnPostoperative pain
- Registration Number
- NL-OMON55379
- Lead Sponsor
- eids Universitair Medisch Centrum
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 47
Inclusion Criteria
ASA class 1-3 patients, aged 18 and older that will undergo an elective
pancreaticoduodenectomy under general anesthesia.
Exclusion Criteria
Patients that are unable to give written informed consent. Patients with a
contra-indication for intravenous morphine, epidural analgesia or sublingual
sufentanil (e.g. allergies, coagulopathies etc.)
Study & Design
- Study Type
- Observational non invasive
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method <p>The main end-point of the study will be *mean pain score during postoperative<br /><br>day 1-3 and mean day pain satisfaction on day 1-3. </p><br>
- Secondary Outcome Measures
Name Time Method