Ketorolac Versus Triamcinolone Knee Injections for Osteoarthritis

Subject Population: Adult patients, age 18-90 years old who satisfy the inclusion criteria and do not meet the exclusion criteria will be enrolled from the Orthopaedics Clinic at San Antonio Military Medical Center (SAMMC). The enrollment period for this study is two years, patients will be recruited up to 44 enrollees to allow 36 completers. Patients will be stratified based on gender and age (< 65 or >= 65 years old). Demographics obtained will be age, gender, height, weight, laterality and body-mass index (BMI).

Randomization: This will be a predetermined computerized randomization schedule to identify treatment, ketorolac tromethamine versus triamcinolone acetonide. A patient key on paper listing the patient name, last four digits of sponsor's social security number, study number (randomly assigned), and treatment will be kept with the nurse/technician in the Orthopaedics Clinic, locked in a cabinet. Patients will be stratified by gender and age (< 65 or >= 65 years old). Subjects will continue to be enrolled until there are at least 10 of each gender in each group, treated with either ketorolac tromethamine or triamcinolone acetonide. In the event the subject has bilateral knee pain, both knees will be injected with the same treatment medication and the knee will be randomized as to which one will be included in the data analysis.

A pharmacist will prepare the treatment injection in the Orthopaedics Clinic. Injections will be done with a 2-inch, 21-gauge needle placed on a 10cc syringe with an opaque covering to conceal its contents to blind the patient and associate investigator to treatment. Injections will contain either 2cc of ketorolac tromethamine (Toradol, 15mg/cc) in 8cc of bupivacaine hydrochloride (0.5%) without epinephrine or 2cc of triamcinolone acetonide (Kenalog-40, 40mg/cc) in 8cc of bupivacaine hydrochloride (0.5%) without epinephrine. The subject and the treatment injection will be taken to the Interdisciplinary Pain Management Center, for injection under ultrasound guidance. The subject's selected knee, or bilateral knees, at the superolateral site, will be sterilely prepped in standard fashion with betadine and allowed to dry, prior to injection. The treatment will be injected by the associate investigator, in the Interdisciplinary Pain Management Center, who is trained in Physical Medicine and Rehabilitation and certified to perform ultrasound examinations. The associate investigator will be blinded to treatment and outcomes.

A patient key listing the patient name, last four digits of sponsor's social security number, age, gender, patient number (randomly assigned) and treatment received will be kept with the nurse/technician in the Orthopaedics Clinic in a research folder, locked in a cabinet.

Radiographs will be obtained at baseline and at 6 months follow-up. Osteoarthritis will be classified according to Kellgren-Lawrence (K-L) radiographic criteria by associate investigator who is fellowship trained in Total Joints. K-L grading will be entered on the Case Report Form (CRF) prior to outcome data entry. The associate investigator will be blinded to treatment. Outcome data collection will be performed by a study nurse/technician in the Orthopaedics Clinic, with the exception of part of the Knee Society Score (KSS), which will be performed by an associate investigator. The nurse/technician will record demographic data, including height, weight, BMI, gender, laterality and age, at the baseline clinic visit and at the 6 month follow-up. The use of nonsteroidal anti-inflammatory drug (NSAID) and analgesic drugs and adverse events during the study period will be recorded at each visit. Patients will keep a diary of NSAID and analgesic use during the study. Patients will follow-up at 2 weeks, 6 weeks, 3 months and 6 months. A visual analogue scale (VAS), KSS, Western Ontario and McMasters Universities (WOMAC) index, Short Form 36 (SF-36), University California Los Angeles (UCLA) Activity Score and Lysholm Knee Score (LKS) will be obtained at the baseline clinic visit and each follow-up. All data obtained from the study will be recorded on the CRF. All data collected will be kept with the nurse/technician in the Orthopaedics Clinic in a research folder, locked in a cabinet.

Data from the CRF will be entered into an electronic database on Excel by the principle investigator on a password protected computer. The database will be made available to the associate investigators electronically. Data analysis will be performed by the principle investigator which will also be performed on a password protected computer. All investigators will remain blinded to the treatment received, until all data analysis is performed. There will be no patient identifiers in the data provided to the investigators, only the patient number. The patient number is a number randomly assigned to the patient and is only identifiable in the patient key, which will be kept separate as above.

A sample size of 16 per group achieve 80% power to detect a difference of 1.6 (16mm) VAS comparing ketorolac tromethamine to triamcinolone acetonide intra-articular injections with estimated standard deviations of 1.56 and with a significance level (alpha) of 0.05. There is an expected drop-out rate of 20%, which implies a sample size of 20 subjects per group. Data analysis will be performed by the principle investigator and associate investigator who will be blinded to treatment until data analysis is complete.