ACTRN12612000343808Not yet recruiting未知
A retrospective/prospective study of patients who had undergone total knee arthroplasty during 2011 and 2012 with a specific pain protocol, analysing outcomes in the post operative period.
Dr Gerald Yeo0 sites100 target enrollmentStarted: March 26, 2012Last updated:
Conditions
Trial Snapshot
- Phase
- 未知
- Status
- Not yet recruiting
- Sponsor
- Enrollment
- 100
Study Overview
Brief Summary
No summary available.
Study Design
- Study Type
- Interventional
- Allocation
- Non-randomised trial
- Primary Purpose
- Treatment
Eligibility Criteria
- Ages
- 50 Years to 100 Years (—)
- Sex
- All
Inclusion Criteria
- •Unilateral total knee arthroplasty at Cairns Base Hospital using the specific pain protocol (GA/spinal + FNB + posterior capsule infiltration)
Exclusion Criteria
- •- Patients not providing informed consent.
- •- Refusal of treatment plan.
- •- Preexisting medical/neurological/hematologic conditions contraindicated for spinal anesthesia or peripheral nerve blocks.
- •- Revision total knee arthroplasty.
- •- Known allergy to any of the medications being used.
- •- History of drug or alcohol abuse.
- •- Patients with chronic pain on slow-release preparations of opioid in excess of 30mg of morphine equivalence per day.
- •- Patients with Rheumatoid Arthritis.
- •- Patients with psychiatric disorders.
- •- Patients unable or unwilling to use Patient Controlled Analgesia.
- •- Obese patients (i.e. BMI >45).
- •- Postoperatively, patients will be excluded if they have had additional operative procedures requiring a change in the usual rehabilitation protocol of care.
Investigators
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