de Haan J J, Goring R L, Beale B S
Department of Small Animal Clinical Sciences, College of Veterinary Medicine, University of Florida, Gainesville.
Vet Surg. 1994 May-Jun;23(3):177-81. doi: 10.1111/j.1532-950x.1994.tb00468.x.
A double-blinded, controlled clinical study was performed to compare the response of adult dogs affected with hip dysplasia to a placebo and three different dosages of polysulfated glycosaminoglycan (PSGAG): 2.2 mg/kg, 4.4 mg/kg, and 8.8 mg/kg. Dogs were randomly assigned to treatment groups. The drug was administered intramuscularly every 3 to 5 days for a total of eight injections. Response to treatment was analyzed based on changes in lameness, range of motion (ROM), and pain on manipulation of the hip joints. Evaluation for adverse reactions included complete blood cell (CBC) count, blood urea nitrogen (BUN), creatinine, and physical examination. Data were collected on a total of 111 dogs. Eighty-four met all criteria for inclusion in the study. Dogs that were given 4.4 mg/kg of PSGAG showed the greatest improvement in orthopedic scores, whereas dogs in the placebo group showed the smallest improvement; however, the differences in clinical improvement between the four treatment groups were not statistically significant. No local or systemic adverse reactions related to the drug were observed.
进行了一项双盲对照临床研究,以比较成年髋关节发育不良犬对安慰剂和三种不同剂量的多硫酸化糖胺聚糖(PSGAG)(2.2毫克/千克、4.4毫克/千克和8.8毫克/千克)的反应。犬被随机分配到治疗组。药物每3至5天肌肉注射一次,共注射八次。根据跛行、活动范围(ROM)和髋关节触诊时的疼痛变化分析治疗反应。不良反应评估包括全血细胞(CBC)计数、血尿素氮(BUN)、肌酐和体格检查。总共收集了111只犬的数据。84只符合研究纳入的所有标准。给予4.4毫克/千克PSGAG的犬在骨科评分上改善最大,而安慰剂组的犬改善最小;然而,四个治疗组之间临床改善的差异无统计学意义。未观察到与药物相关的局部或全身不良反应。