Spinal or hemi-spinal anesthesia in fast-track total hip arthroplasty and total knee arthroplasty (THA and TKA), a prospective randomized controlled study in the Martini Hospital
Completed
- Conditions
- anesthesie technieken bij orthopedische patientenspinal anesthesia versus hemi-spinal anesthesia
- Registration Number
- NL-OMON40716
- Lead Sponsor
- Martini Ziekenhuis
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 600
Inclusion Criteria
primary TKA or THA
patients older than 18 year
Exclusion Criteria
not a primary THA or TKA
patients with a strong preferance for one or the two anesthesia methods
patient who want general anesthesia
patient with a contra-indication for spinal anesthesia
Study & Design
- Study Type
- Observational non invasive
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method <p>The main endpoint is conversion to general anesthesia which is a measure for<br /><br>effectiveness of (hemi-)spinal anesthesia.</p><br>
- Secondary Outcome Measures
Name Time Method <p>Secondary outcomes are length of stay in the post anesthesia care unit (PACU),<br /><br>need for urinary catheterization, intra operative blood loss, motoric<br /><br>dysfunction, postoperative pain and opioid consumption, orthostatic intolerance<br /><br>and dizziness, postoperative nausea and vomiting, reduction in length of stay<br /><br>(LOS)</p><br>