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Randomized Controlled Trial
The analgesic efficiency of pregabalin for the treatment of postoperative pain in total hip arthroplasty: A randomized controlled study protocol.
- Yuangui Zhang, Xiaoqian Wang, and Guimin Dong.
- Department of Anesthesiology, Weifang People's Hospital, Shandong 261000, China.
- Medicine (Baltimore). 2020 Jul 2; 99 (27): e21071.
BackgroundOnly few studies have yet investigated whether perioperative administration of pregabalin can reduce the incidence of postoperative chronic neuropathic pain after total hip arthroplasty (THA). This prospective, randomized study compared placebo with pregabalin in the hope that a lower pregabalin dose would improve analgesia without increasing side-effects after THA.MethodsThis study was a prospective randomized blinded study, with a parallel design and an allocation ratio of 1:1 for the treatment groups. The study was approved by the Institutional Review Board in Weifang People's Hospital and written informed consent was obtained from all subjects before enrolment. A total of 120 patients who meet inclusion criteria are randomized to either pregabalin or placebo group. The primary objective of the study was visual analog scale score. As secondary outcomes, opioid consumption measurement, Harris Hip Score, hip range of motion, patient satisfaction, and complications were made at different time points throughout the study for comparison.ResultsThe null hypothesis of this study was that pregabalin would reduce pain after THA.Trial RegistrationThis study protocol was registered in Research Registry (researchregistry5669).
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