Postoperatieve pijnbehandeling middels continue epidurale toediening van bupivacaïne/sufentanil versus bupivacaïne/morfine bij patiënten na een grote chirurgische ingreep.
Recruiting
- Conditions
- epidural, bupivacaïne, sufentanil, morphine, analgesia, side effectsEpiduraal, morfine, analgesie, bijwerkingen
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Not specified
- Target Recruitment
- 424
Inclusion Criteria
1. Age 18 years or older;
2. Scheduled major surgery;
Exclusion Criteria
1. Patients with an allergy to one of the study medications;
2. Patients using opioids pre-operatively;
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The pain scores during the first 72 hours after surgery.
- Secondary Outcome Measures
Name Time Method The quality of pain relief (as experienced by the patient) and side/adverse effects: pruritis, drowsiness, nausea, vomiting and/or motor block, sedation, respiratory depression and episodes of hypotension.