Petrella 2015.
Methods | Randomised controlled trial 2‐arm parallel‐group design Trial duration: 26 weeks |
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Participants | 98 participants with knee osteoarthritis were randomised 98 participants were reported at baseline Number of females: 56 out of 98 (57%) Mean age: 59.7 years |
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Interventions |
Experimental intervention 10 mg triamcinolone acetonide + hyaluronan solution (no dosage stated), 6 ml total, single intra‐articular injection Control intervention Hyaluronan solution (no dosage stated), single intra‐articular injection |
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Outcomes | Extracted pain outcome: WOMAC Pain Extracted function outcome: WOMAC Function Maximum follow‐up: 26 weeks |
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Notes | Funding: Carbylan Therapeutics | |
Risk of bias | ||
Bias | Authors' judgement | Support for judgement |
Random sequence generation (selection bias) | Low risk | Quote: "The randomization treatment was computer generated and was stratified by study center." |
Allocation concealment (selection bias) | Unclear risk | Quote: "The randomization treatment was computer generated and was stratified by study center." |
Blinding of participants? | Unclear risk | It was unclear if method used to blind participants was appropriate |
Blinding of health care provider(s) | High risk | Quote: "An injecting physician delivered the randomized treatment and remained unblinded." |
Intention‐to‐treat analysis performed? Pain | High risk | 2 of 33 participants excluded in experimental group, 1 of 33 participants excluded in control group |
Intention‐to‐treat analysis performed? Function | High risk | 2 of 33 participants excluded in experimental group, 1 of 33 participants excluded in control group |