Safety and efficacy of letibotulinumtoxinA(BOTULAX®) in treatment of post stroke upper limb spasticity: a randomized, double blind, multi-center, phase III clinical trial

被引:10
作者
Do, Kyung Hee [1 ]
Chun, Min Ho [2 ]
Paik, Nam-Jong [3 ,4 ]
Park, Yoon Ghil [5 ]
Lee, Shi-Uk [3 ,6 ]
Kim, Min-Wook [7 ]
Kim, Don-Kyu [8 ]
机构
[1] Vet Hlth Serv Med Ctr, Dept Phys Med & Rehabil, Seoul, South Korea
[2] Univ Ulsan, Coll Med, Asan Med Ctr, Dept Phys Med & Rehabil, 88 Olymp Ro 43 Gil, Seoul 05505, South Korea
[3] Seoul Natl Univ, Coll Med, Dept Rehabil, Seoul, South Korea
[4] Seoul Natl Univ, Bundang Hosp, Dept Rehabil, Seongnam, South Korea
[5] Yonsei Univ, Coll Med, Inst Neuromuscular Dis, Dept Rehabil Med & Rehabil, Seoul, South Korea
[6] Seoul Natl Univ, Boramae Med Ctr, Dept Phys Med & Rehabil, Seoul, South Korea
[7] Catholic Univ Korea, Incheon St Marys Hosp, Coll Med, Dept Phys Med & Rehabil, Incheon, South Korea
[8] Chung Ang Univ, Coll Med, Dept Phys Med & Rehabil, Seoul, South Korea
关键词
Spasticity; stroke; botulinum neurotoxin type A; efficacy; safety; TOXIN TYPE-A; PLACEBO-CONTROLLED TRIAL; BOTULINUM TOXIN; ASHWORTH SCALE; ARM SPASTICITY; OPEN-LABEL; INJECTION; RELIABILITY; NEUROTOXIN; INTERRATER;
D O I
10.1177/0269215516689331
中图分类号
R49 [康复医学];
学科分类号
100215 ;
摘要
Objective: To investigate a new botulinum neurotoxin type A, termed letibotulinumtoxinA(Botulax((R))) and compare its efficacy and safety for post-stroke upper limb spasticity with that of onabotulinumtoxinA(Botox((R))). Design: A prospective, double-blinded, multicenter, randomized controlled clinical study. Setting: Six university hospitals in Korea. Subjects: A total of 187 stroke participants with upper limb spasticity. Interventions: Two kinds of botulinum neurotoxin type A were used. One set of injection was performed and total injected doses were 309.2162.48U(Botulax) and 312.6449.99U(Botox)(P>0.05). Main measures: Primary outcome was measured using the modified Ashworth scale for wrist flexors at week 4 and secondary outcome was measured using modified Ashworth scale for wrist flexors, elbow flexors, finger flexors, and thumb flexors as well as Global Assessment in spasticity, Disability Assessment Scale, and Caregiver Burden Scale. Safety measures including adverse events, vital signs and physical examination, and laboratory tests were also monitored. Results: The mean ages for the Botulax group were 56.81 +/- 9.49 and which for the Botox group were 56.93 +/- 11.93(P>0.05). In primary outcome, the change in modified Ashworth scale for wrist flexors was -1.45 +/- 0.61 in the Botulax group and -1.40 +/- 0.57 in the Botox group, and the difference between the two groups was -0.06(95% CI:-0.23-0.12,P>0.05). In secondary outcome, both groups demonstrated significant improvements with respect to modified Ashworth scale, Global Assessment in spasticity, Disability Assessment Scale, and Caregiver Burden Scale (P<0.05), and no significant difference was observed between the two groups (P>0.05). In addition, safety measures showed no significant differences between the two groups (P>0.05). Conclusions: The efficacy and safety of Botulax were comparable with those of Botox in treatment of post-stoke upper limb spasticity.
引用
收藏
页码:1179 / 1188
页数:10
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