The PanAM study: A multi-center, double-blinded, randomized, non-inferiority study of paracetamol versus non-steroidal anti-inflammatory drugs in treating acute musculoskeletal trauma

被引:9
|
作者
Ridderikhof M.L. [1 ]
Lirk P. [2 ]
Schep N.W. [3 ]
Hoeberichts A. [4 ]
Goddijn W.T. [1 ]
Luitse J.S.K. [1 ]
Kemper E.M. [5 ]
Dijkgraaf M.G. W. [6 ]
Hollmann M.W. [2 ]
Goslings J.C. [3 ]
机构
[1] Department of Emergency Medicine, Academic Medical Center, 1100 DD, Amsterdam
[2] Department of Anaesthesiology, Academic Medical Center, 1100 DD, Amsterdam
[3] Trauma Unit Department of Surgery, Academic Medical Center, 1100 DD, Amsterdam
[4] General Practice Health Care Center Gein, 1106 MH, Amsterdam
[5] Department of Pharmacy, Academic Medical Center, 1100 DD, Amsterdam
[6] Clinical Research Unit, Academic Medical Center, 1100 DD, Amsterdam
关键词
Analgesia; Anti-inflammatory agents; Contusions; Costs and cost analysis; Non-steroidal; Pain; Paracetamol/acetaminophen; Strains and sprains; Wounds and injuries;
D O I
10.1186/1471-227X-13-19
中图分类号
学科分类号
摘要
Background: Acute musculoskeletal trauma, including strains, sprains or contusions, occur frequently. Pain management is a crucial component of treatment. However, there is no convincing evidence which drug is superior in managing pain in these patients. The aim of the PanAM Study is to compare analgesic efficacy of three strategies of pain management: paracetamol, diclofenac, or a combination of both in patients with acute musculoskeletal trauma.Methods/design: The PanAM Study is a multi-center, double blind randomized controlled trial with non-inferiority design. Included are adult patients presenting to an academic, urban Emergency Department or to a General Practice with acute, blunt, traumatic limb injury. In total, 547 patients will be included using a predefined list of exclusion criteria, to be allocated by randomization to treatment with paracetamol + placebo diclofenac, diclofenac + placebo paracetamol or paracetamol + diclofenac. The hypothesis is that paracetamol will not be inferior to treatment with diclofenac, or the combination of both. Primary outcome will be between-group differences in decrease in pain, measured with Numerical Rating Scales at baseline and at 90 minutes after study drug administration. Secondary outcomes are Numerical Rating Scales at 30 and 60 minutes and measured frequently during three consecutive days after discharge; occurrence of adverse effects; patient satisfaction and an analysis of quality of life and cost-effectiveness. Recruitment started July 2013 and is expected to last a year.Discussion: With this multi-center randomized clinical trial we will investigate whether treatment with paracetamol alone is not inferior to diclofenac alone or a combination of both drugs in adult patients with acute musculoskeletal trauma. The main relevance of the trial is to demonstrate the benefits and risks of three commonly used treatment regimens for musculoskeletal trauma. Data that lead to the prevention of severe Non-Steroidal Anti-Inflammatory Drugs-related adverse effects might be gathered.Trial registration: Dutch Trial Register (http://www.trialregister.nl): NTR3982.EudraCT database (http://www.clinicaltrialsregister.eu): 201300038111. © 2013 Ridderikhof et al.; licensee BioMed Central Ltd.
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