Total Hip Arthroplasty: Multiple Blocks by UltraSound (THAMBUS)
Pain, Postoperative
About this trial
This is an interventional treatment trial for Pain, Postoperative focused on measuring Hip arthroplasty, Peripheral nervous blockade, Postoperative, Pain, Ropivacaine
Eligibility Criteria
Inclusion Criteria:
- Minimum 18 years of age
- Patients scheduled for primary, unilateral hip arthroplasty with spinal anaesthesia
- Patients who have given their written and informed consent to participation after having understood the content and limitations of the protocol fully
- ASA 1-3
Exclusion Criteria:
- Patients who are not able to co-operate
- Patients who do not speak or understand Danish
- Daily use of opioids corresponding to 40 mg of morphine daily
- Allergy towards the drugs used in the study
- Drug abuse (investigators judgement)
- Alcohol consumption larger than advised by the Danish National Board of Health
- Spinal anaesthesia is contraindicated or the patient wants a general anaesthesia
- Patients in whom the blockade procedure or the spinal anaesthesia procedure cannot be completed because of technical difficulties
Sites / Locations
- Bispebjerg HospitalRecruiting
Arms of the Study
Arm 1
Arm 2
Arm 3
Active Comparator
Active Comparator
Sham Comparator
B3: Blockade of three nerves
B2: Blockade of 2 nerves
K: Control group
Peripheral nerve blockade of the femoral nerve, the anterior division of the obturator nerve, and the lateral femoral cutaneous nerve with ropivacaine.
Peripheral nerve blockade of the anterior division of the obturator nerve and the lateral femoral cutaneous nerve with ropivacaine. Sham blockade of the femoral nerve with saline.
Sham blockade of the femoral nerve, the anterior division of the obturator nerve, and the lateral femoral cutaneous nerve with saline.