ocal Infiltration Anaesthesia in Total Hip Arthroplasty by Anterior Supine Intermuscular Approach
Phase 2
Completed
- Conditions
- pain after total hip arthroplasty10023213
- Registration Number
- NL-OMON39407
- Lead Sponsor
- Reinier de Graaf Groep
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 75
Inclusion Criteria
The hospital criteria for patients diagnosted for a total hip arthroplasty with osteoarthritis will be applied
* Patients aged 18 years and older.
* Patients willing to participate.
* ASA I and II.
Exclusion Criteria
* Patients unwilling to participate.
* Mentally retarded.
* Neurological conditions potentially influence pain perception.
* Psychiatric conditions potentially influence pain perception.
* ASA III, IV and V.
* Cardiovascular impairment inthe present and the past.
* Abuse of alcohol or drugs.
* Known allergy for any element of the medication that is given (ropivacain, epinephrin).
* Medical contra indication for spinal anaesthesia.
* BMI > 40.
* Rheumatoid arthritis.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method <p>- Pain score (NRS) at day 1 at multiple moments: 1, 4 and 8 hours after<br /><br>operation in rest, and while and direct after mobilization starting at 4-6<br /><br>hours after operation. At day 2 until the day of discharge at two moments. Also<br /><br>during and immediately after mobilization.<br /><br>- Preoperative pain will be scored during the preoperative<br /><br>screening.<br /><br>- POVN is asked at the moments the VAS is scored.<br /><br>- Cumulative consumption of opioid medication and pain medication.<br /><br>- Length of Hospital Stay by amount of nights and number of hours between<br /><br>operation and discharge.</p><br>
- Secondary Outcome Measures
Name Time Method <p>not applicable</p><br>