Postoperative Pain Relief Following Total Hip Arthroplasty. A Comparison Between Intrathecal Morphine (IM) and Local Infiltration Analgesia (LIA) (HÖFTPLASTIK)
Recruitment status was Recruiting
|First Received Date ICMJE||January 20, 2011|
|Last Updated Date||September 11, 2012|
|Start Date ICMJE||September 2009|
|Estimated Primary Completion Date||September 2012 (final data collection date for primary outcome measure)|
|Current Primary Outcome Measures ICMJE
||Total morphine consumption postoperatively [ Time Frame: During 0 -24 hours postoperatively ] [ Designated as safety issue: Yes ]
Other than total morphine consumption, even pain intensity on movement would be considered to be an important parallel end-point.
|Original Primary Outcome Measures ICMJE||Same as current|
|Change History||Complete list of historical versions of study NCT01281891 on ClinicalTrials.gov Archive Site|
|Current Secondary Outcome Measures ICMJE
||Pain intensity (NRS, Numeric Rating Score; 0-10) [ Time Frame: 0 - 24 h ] [ Designated as safety issue: No ]|
|Original Secondary Outcome Measures ICMJE||Same as current|
|Current Other Outcome Measures ICMJE||Not Provided|
|Original Other Outcome Measures ICMJE||Not Provided|
|Brief Title ICMJE||Postoperative Pain Relief Following Total Hip Arthroplasty. A Comparison Between Intrathecal Morphine (IM) and Local Infiltration Analgesia (LIA)|
|Official Title ICMJE||Postoperative Pain Relief Following Total Hip Arthroplasty. A Comparison Between Intrathecal Morphine (IM) and Local Infiltration Analgesia (LIA)|
Postoperative pain following total hip arthroplasty (THA) (1) is often considered moderate to severe and can therefore influence the postoperative course of event and result in delayed postoperative mobilization and prolonged hospitalization. It is therefore necessary to find the most optimal method for alleviation of pain for these patients. Traditionally, this has been managed by epidural analgesia, continuous peripheral nerve blocks, parental- or spinal opioids. Recently, Drs Kerr and Kohan at the Joint Orthopaedic Centre in Sydney, Australia developed a local infiltration analgesia (LIA) technique. The technique was introduced in Scandinavia during 2001 and has been shown to be efficacious during knee surgery. The LIA technique is based on a systemic infiltration of a mixture of a long-acting local anaesthetic (ropivacaine), a non steroidal anti-inflammatory drug (ketorolac), and epinephrine into the tissue around the surgical field to achieve satisfactory pain control with little physiological disturbance. A catheter is left from the skin and into the joint cavity, allowing repeated injection on the morning after surgery (10). Effective pain relief with early mobilization and reduced hospital stay has been reported following total knee arthroplasty and, recently, following unicompartmental knee arthroplasty.
The aim of this study is to assess whether LIA technique is equi-efficacious to intrathecal morphine, the standard of care in our hospital.
This is a randomized, double blind parallel-group study where two different methods for postoperative pain relief after total hip arthroplasty, intrathecal morphine (IM) and local infiltration analgesia (LIA), will be assessed.
The study will be conducted at the Department of Anaesthesiology and Intensive Care and the Department of Orthopaedic Surgery, at USÖ. A total of 80 patients undergoing total hip arthroplasty will be included in the study, 40 patients in group IM and 40 patients in group LIA. The patients will be divided into one of the two groups according to computer-generated randomization. Study duration per patient will be 6 months.
Screening on the basis of inclusion and exclusion criteria will take place at the preoperative assessment at the outpatients' anesthesia clinic 3 - 6 weeks before the total hip arthroplasty. One of the participating investigators will inform the patient, both verbally and in writing, about what participation in the study involves. The patient will be given time to ask questions and to consider participation in the study.
If the patient wants to be enrolled in the study, inclusion will take place at the preoperative assessment that takes place before the total hip arthroplasty. One of the participating Investigators would inform the patient again about what participation in the study means. The patient will be given time to ask questions and to consider participation in the study. The patient can be enrolled in the study after signing and dating the written Informed Preoperative Preparation The patients will be informed in details about the surgery, anesthesia, postoperative pain relief and physiotherapy. All patients will be asked to complete two health related quality of life questionnaires, SF-36 and EQ5D (appendix 2 and 3).
A baseline value for HOOS (appendix 4) and NRS (Numeric Rating Score) will be assessed prior to surgery. The patients will also be instructed on how to use the patient controlled analgesia (PCA) morphine pump that will serve as post-operative rescue medication in case of pain > 3 on the numeric rating scale (NRS) Dalteparin 5000 IU is administered subcutaneously once each evening for 10 days, starting the night before surgery for thrombo-prophylaxis.
Randomisation Randomisation will be made at the USÖ Hospital Pharmacy the day before surgery. The patients will be randomized into two groups, 40 patients in Group IM and 40 patients in Group LIA, according to computer-generated randomization.
The study medication/saline will be prepared, blinded and labeled by a pharmacist at the USÖ Hospital Pharmacy. The hospital pharmacy will send the double-blinded study medication/saline to the operating theater on the day of surgery. This way, double blinding will be ensured such that neither the patient nor the anaesthesiologists, the staff attending the surgery, the staff concerned with the postoperative care of the patients or the physiotherapist are aware of the group to which the patient has been randomized. The study medication/saline will be stored in room temperature in the operating theatre and will be given within one hour from the time it is received. Study medication/saline for the peri-articular injection on postoperative day one will be kept in a refrigerator at the Department of Anesthesiology and intensive care until it is to be given.
Anaesthesia All patients will receive a mixture of midazolam 0.03 mg/kg orally 1 hour before planned surgery. Cloxacillin 1g will be given intravenously before surgery and at 8, 16 and 24 h postoperatively. The operation will be performed using spinal anaesthesia, performed in the sitting position, using a 27G spinal needle. All patients will receive bupivacaine plain 5 mg/ml (17.5 mg = 3.5 ml) injected intrathecally. In addition, patients randomized to Group IM will receive morphine special 0.4 mg/ml (0.1 mg =0.25 ml) and patients randomized to Group LIA will receive an equivalent amount (= 0.25 ml) of normal saline. Total volume of injectate will for each patient be 3.75 ml.
Surgery and Perioperative Management The surgery will be performed in a standardized way according to routine at Örebro University hospital. At the end of surgery, and after the hip prosthesis is in place, patients in Group LIA would receive a total volume of 151.5 ml of a mixture consisting of: a long-acting local anaesthetic (ropivacaine 2 mg/ml = 150 ml), a no-steroidal anti-inflammatory drug (ketorolac 30 mg/ml = 1 ml), and epinephrine (1 mg/ml = 0.5 ml) injected intraarticularly and into the surrounding peri-articular tissues in a standardized way. Patients in Group IM would receive a similar volume (151.5 ml) of normal saline injected in the same way at similar sites in order to ensure double-blinding of all personnel involved in the study.
A multi-holed catheter (a peri-articular catheter) would be inserted into the tissue planes under direct vision in a standardized way before closing the wound and would be connected to a bacterial filter under sterile conditions. After the surgery the patient would be transferred to the post-anaesthesia care unit (PACU) and thereafter to the orthopaedic ward for further management.
During the first post-operative day, 24 hours after surgery the following solutions will be injected peri-articularly via the multi-holed catheter by a nurse who is blinded to the injectate:
20 ml of ropivacaine (7.5 mg/ml)
1 ml ketorolac (30 mg/ml)
1 ml of epinephrine (0.1 mg/ml)
22 ml saline
Total volume of injectate will for each patient be 22 ml.
The multi-holed catheter would then be removed and the tip of the catheter sent for culture and sensitivity testing. Any evidence of fever or local or systemic infection will be recorded.
Pain Management All patients will receive 1 g paracetamol orally 4 times a day, starting on the morning of the operation.
A patient controlled analgesia (PCA) morphine pump (1 mg bolus dose, 6 min lock-out time) would be connected IV in all patients, and will serve as rescue medication in case of pain > 3 on the numeric rating scale (NRS; 0 = no pain, 10 = worst imaginable pain). The patients will be instructed on its use the day before surgery. If pain is < 4 during a 12 h period, the PCA-pump will be discontinued and tramadol 50 mg given orally up to 4 times/day as necessary as rescue medication for pain management. All patients would receive Paracetamol 1 g six-hourly as basal analgesic.
Mobilization and Home discharge The first attempt to mobilization will be made about 30 min after the peri-articularly injection of study medication/saline, 24 h after surgery. The patient will be asked to stand up and to walk 10 steps. If unsuccessful, another attempt will be made to mobilize the patient every 12 h until the patient can walk 10 steps. If the 12 h period is after 9 pm, the next attempt would be made on the following morning. Subsequently, mobilization will also be quantified using a TUG test (appendix 5) from postoperative day 1 until discharge
The patient will be discharged when the discharge criteria are fulfilled:
The patient will also be asked to register pain (NRS) and analgesic consumption during the first 14 postoperative days and at week 2, 3 and 4. (appendix 6)
Recordings and Assessments (Flowchart, appendix 7)
Age, gender, height and weight.
Length of stay at the hospital (LOS):
The number of postoperative days to home discharge, day 0 = the day of surgery would be recorded.
Home discharge criteria are:
Pain assessment will be recorded by NRS scale preoperatively and at 1, 4, 8, 12, 24, 36 and 48 hours postoperative, subsequently every 24 hour until the patient is discharged from hospital, on day 14 and 3 and 6 months postoperatively.
Pain will be assessed both at rest and on motion (after walking 10 steps).
Morphine consumption will be recorded during 0 - 4, 4 - 24 and 24-48 hours postoperatively.
Oral analgesic consumption will be recorded each day until home discharge. The patients will be asked to record their pain and analgesic consumption once each day for 14 days and weekly on weeks 2, 3 and 4.
The research nurse or physiotherapist will record the hip extension and flexion every 24 h until discharge and after 14 days, 3 and 6 months postoperatively.
TUG test will be performed från postoperative day 1 until discharge Patient satisfaction during the first 24 postoperative hours and after 7 days will be rated according to a satisfaction score: 1= poor, 2= satisfactory, 3= good and 4= excellent.
HOOS will be collected preoperatively, and at 2 weeks, 3 and 6 months postoperatively.
The SF-36 and EuroQol (EQ-5D) questionnaires will be collected preoperatively and postoperatively on day 7 (only EQ-5D), 3 and 6 months.
The SF-36 is a validated health survey consisting of 36 questions that measure 8 health concepts: physical functioning (PF), role limitations due to physical problems (RP), bodily pain (BP), general health (GH), vitality (VT), social functioning (SF), role limitations secondary to emotional problems (RE) and mental health (MH). Additionally, 2 summary scores are available: a standardized physical component (PCS) and a standardized mental component (MCS).
The EuroQol (EQ-5D) is a standardised instrument for use as a measure of health outcome. It provides a single index value from 0 to 1 where 0 represents death and 1 represents perfects health.
|Study Type ICMJE||Interventional|
|Study Phase||Phase 4|
|Study Design ICMJE||Allocation: Randomized
Endpoint Classification: Safety/Efficacy Study
Intervention Model: Parallel Assignment
Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor)
Primary Purpose: Treatment
|Condition ICMJE||Primary Osteoarthritis Requiring Total Hip Replacement|
|Study Arm (s)||
|Publications *||Not Provided|
* Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
|Recruitment Status ICMJE||Recruiting|
|Estimated Enrollment ICMJE||80|
|Estimated Completion Date||September 2012|
|Estimated Primary Completion Date||September 2012 (final data collection date for primary outcome measure)|
|Eligibility Criteria ICMJE||
|Ages||50 Years to 85 Years|
|Accepts Healthy Volunteers||No|
|Listed Location Countries ICMJE||Sweden|
|Removed Location Countries|
|NCT Number ICMJE||NCT01281891|
|Other Study ID Numbers ICMJE||THA001|
|Has Data Monitoring Committee||Yes|
|Plan to Share Data||Not Provided|
|IPD Description||Not Provided|
|Responsible Party||Per Essving, University Hospital Orebro|
|Study Sponsor ICMJE||University Hospital Orebro|
|Collaborators ICMJE||Not Provided|
|Investigators ICMJE||Not Provided|
|Information Provided By||University Hospital Orebro|
|Verification Date||September 2012|
ICMJE Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP