Remifentanil use for sedation and pain managment during a painful treatment at the emergency department.
Recruiting
- Conditions
- remifentanil, target controlled infusion, procedural sedation, analgesia, recovery time, emergency department, propofol, fentanyl.procedurele sedatie, pijnstilling, hersteltijd, spoedeisende hulp.
- Registration Number
- NL-OMON28296
- Lead Sponsor
- Albert Schweitzer hospital, Dordrecht, The NetherlandsM.A.A. van Hooft
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Not specified
- Target Recruitment
- 60
Inclusion Criteria
All the patients who need procedural sedation and analgesia at the emergency department or the observatorium of the Albert Schweitzer hospital location Dordwijk in Dordrecht, age 18 years and older, classified as ASA I en II.
Exclusion Criteria
Age under 18 years, hemodynamic and/or respiratory instable, classified as ASA III, IV and V, suspicion of elevated intra-cranial pressure, pregnancy, use of opiates at home, opiates administered before PSA procedure started (in the ambulance, on arrival at the emergency department), intoxication, known allergy for fentanyl propofol remifentanil soy or chicken proteins.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The recovery time ( time between last dose PSA medication and full recovery of the patient).
- Secondary Outcome Measures
Name Time Method - Adverse effects, complications.<br /><br>- Succesfull interventions.<br /><br>- Satisfaction of the specialist about performing the intervention. <br /><br>- Adequate analgesia during procedure. <br /><br>- Satisfaction patient.